Canonical Allele Identifier: CA2392195579

Gene: COL18A1 SLC19A1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.45510961_45511020delinsATACACCCCCAAACACCCCCCACACCCCACACACACAACACACCCCCCCCCCACACATCC , CM000683.2:g.45510961_45511020delinsATACACCCCCAAACACCCCCCACACCCCACACACACAACACACCCCCCCCCCACACATCC	GRCh38
NC_000021.8:g.46930875_46930934delinsATACACCCCCAAACACCCCCCACACCCCACACACACAACACACCCCCCCCCCACACATCC , CM000683.1:g.46930875_46930934delinsATACACCCCCAAACACCCCCCACACCCCACACACACAACACACCCCCCCCCCACACATCC	GRCh37
NC_000021.7:g.45755303_45755362delinsATACACCCCCAAACACCCCCCACACCCCACACACACAACACACCCCCCCCCCACACATCC	NCBI36
NG_011903.1:g.110770_110829delinsATACACCCCCAAACACCCCCCACACCCCACACACACAACACACCCCCCCCCCACACATCC
NG_028278.2:g.57124_57183delinsGGATGTGTGGGGGGGGGGTGTGTTGTGTGTGTGGGGTGTGGGGGGTGTTTGGGGGTGTAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000355480.10:c.4234-150_4234-91delinsATACACCCCCAAACACCCCCCACACCCCACACACACAACACACCCCCCCCCCACACATCC (COL18A1)	ENSP00000347665.5:n.4234-150_4234-91delinsATACACCCCCAAACACCCC...
ENST00000651438.1:c.3694-150_3694-91delinsATACACCCCCAAACACCCCCCACACCCCACACACACAACACACCCCCCCCCCACACATCC (COL18A1) MANE Select	ENSP00000498485.1:n.3694-150_3694-91delinsATACACCCCCAAACACCCC...
ENST00000342220.9:c.1738-150_1738-91delinsATACACCCCCAAACACCCCCCACACCCCACACACACAACACACCCCCCCCCCACACATCC (COL18A1)	ENSP00000339118.5:n.1738-150_1738-91delinsATACACCCCCAAACACCCC...
ENST00000355480.9:c.4234-150_4234-91delinsATACACCCCCAAACACCCCCCACACCCCACACACACAACACACCCCCCCCCCACACATCC (COL18A1)	ENSP00000347665.5:n.4234-150_4234-91delinsATACACCCCCAAACACCCC...
ENST00000359759.8:c.4939-150_4939-91delinsATACACCCCCAAACACCCCCCACACCCCACACACACAACACACCCCCCCCCCACACATCC (COL18A1)	ENSP00000352798.4:n.4939-150_4939-91delinsATACACCCCCAAACACCCC...
ENST00000400337.6:c.3694-150_3694-91delinsATACACCCCCAAACACCCCCCACACCCCACACACACAACACACCCCCCCCCCACACATCC (COL18A1)	ENSP00000383191.2:n.3694-150_3694-91delinsATACACCCCCAAACACCCC...
ENST00000417954.5:c.498-12408_498-12349delinsGGATGTGTGGGGGGGGGGTGTGTTGTGTGTGTGGGGTGTGGGGGGTGTTTGGGGGTGTAT (SLC19A1)
ENST00000423214.1:c.648-150_648-91delinsATACACCCCCAAACACCCCCCACACCCCACACACACAACACACCCCCCCCCCACACATCC (COL18A1)
ENST00000473212.1:n.2020-150_2020-91delinsATACACCCCCAAACACCCCCCACACCCCACACACACAACACACCCCCCCCCCACACATCC (COL18A1)
ENST00000567670.5:c.1294-12408_1294-12349delinsGGATGTGTGGGGGGGGGGTGTGTTGTGTGTGTGGGGTGTGGGGGGTGTTTGGGGGTGTAT (SLC19A1)	ENSP00000457278.1:n.1294-12408_1294-12349delinsGGATGTGTGGGGGG...
NM_030582.3:c.4225-150_4225-91delinsATACACCCCCAAACACCCCCCACACCCCACACACACAACACACCCCCCCCCCACACATCC (COL18A1)	NP_085059.2:n.4225-150_4225-91delinsATACACCCCCAAACACCCCCCACAC...
NM_130444.2:c.4930-150_4930-91delinsATACACCCCCAAACACCCCCCACACCCCACACACACAACACACCCCCCCCCCACACATCC (COL18A1)	NP_569711.2:n.4930-150_4930-91delinsATACACCCCCAAACACCCCCCACAC...
NM_130445.3:c.3685-150_3685-91delinsATACACCCCCAAACACCCCCCACACCCCACACACACAACACACCCCCCCCCCACACATCC (COL18A1)	NP_569712.2:n.3685-150_3685-91delinsATACACCCCCAAACACCCCCCACAC...
XM_011529707.1:c.1585-8051_1585-7992delinsGGATGTGTGGGGGGGGGGTGTGTTGTGTGTGTGGGGTGTGGGGGGTGTTTGGGGGTGTAT (SLC19A1)	XP_011528009.1:n.1585-8051_1585-7992delinsGGATGTGTGGGGGGGGGGT...
XM_017028445.2:c.1585-8051_1585-7992delinsGGATGTGTGGGGGGGGGGTGTGTTGTGTGTGTGGGGTGTGGGGGGTGTTTGGGGGTGTAT (SLC19A1)	XP_016883934.1:n.1585-8051_1585-7992delinsGGATGTGTGGGGGGGGGGT...
NM_030582.4:c.4225-150_4225-91delinsATACACCCCCAAACACCCCCCACACCCCACACACACAACACACCCCCCCCCCACACATCC (COL18A1)	NP_085059.2:n.4225-150_4225-91delinsATACACCCCCAAACACCCCCCACAC...
NM_130444.3:c.4930-150_4930-91delinsATACACCCCCAAACACCCCCCACACCCCACACACACAACACACCCCCCCCCCACACATCC (COL18A1)	NP_569711.2:n.4930-150_4930-91delinsATACACCCCCAAACACCCCCCACAC...
NM_130445.4:c.3685-150_3685-91delinsATACACCCCCAAACACCCCCCACACCCCACACACACAACACACCCCCCCCCCACACATCC (COL18A1)	NP_569712.2:n.3685-150_3685-91delinsATACACCCCCAAACACCCCCCACAC...
NM_001379500.1:c.3694-150_3694-91delinsATACACCCCCAAACACCCCCCACACCCCACACACACAACACACCCCCCCCCCACACATCC (COL18A1) MANE Select	NP_001366429.1:n.3694-150_3694-91delinsATACACCCCCAAACACCCCCCA...