Canonical Allele Identifier: CA1022830460

Gene: COL18A1 SLC19A1

Linked Data

• gnomAD v3: 21-45510939-ACACACACCCACAACACCCCACATACACCCCCAAACACCCCCCACACCCCACACACACAACACACCCCCCCCCCACACATCCACACCCCACATC-A
• gnomAD v4: 21-45510939-ACACACACCCACAACACCCCACATACACCCCCAAACACCCCCCACACCCCACACACACAACACACCCCCCCCCCACACATCCACACCCCACATC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.45510949_45511041del , CM000683.2:g.45510949_45511041del	GRCh38
NC_000021.8:g.46930863_46930955del , CM000683.1:g.46930863_46930955del	GRCh37
NC_000021.7:g.45755291_45755383del	NCBI36
NG_011903.1:g.110758_110850del
NG_028278.2:g.57112_57204del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355480.10:c.4234-162_4234-70del (COL18A1)	ENSP00000347665.5:n.4234-162_4234-70del
ENST00000651438.1:c.3694-162_3694-70del (COL18A1) MANE Select	ENSP00000498485.1:n.3694-162_3694-70del
ENST00000342220.9:c.1738-162_1738-70del (COL18A1)	ENSP00000339118.5:n.1738-162_1738-70del
ENST00000355480.9:c.4234-162_4234-70del (COL18A1)	ENSP00000347665.5:n.4234-162_4234-70del
ENST00000359759.8:c.4939-162_4939-70del (COL18A1)	ENSP00000352798.4:n.4939-162_4939-70del
ENST00000400337.6:c.3694-162_3694-70del (COL18A1)	ENSP00000383191.2:n.3694-162_3694-70del
ENST00000417954.5:c.498-12420_498-12328del (SLC19A1)
ENST00000423214.1:c.648-162_648-70del (COL18A1)
ENST00000473212.1:n.2020-162_2020-70del (COL18A1)
ENST00000567670.5:c.1294-12420_1294-12328del (SLC19A1)	ENSP00000457278.1:n.1294-12420_1294-12328del
NM_030582.3:c.4225-162_4225-70del (COL18A1)	NP_085059.2:n.4225-162_4225-70del
NM_130444.2:c.4930-162_4930-70del (COL18A1)	NP_569711.2:n.4930-162_4930-70del
NM_130445.3:c.3685-162_3685-70del (COL18A1)	NP_569712.2:n.3685-162_3685-70del
XM_011529707.1:c.1585-8063_1585-7971del (SLC19A1)	XP_011528009.1:n.1585-8063_1585-7971del
XM_017028445.2:c.1585-8063_1585-7971del (SLC19A1)	XP_016883934.1:n.1585-8063_1585-7971del
NM_030582.4:c.4225-162_4225-70del (COL18A1)	NP_085059.2:n.4225-162_4225-70del
NM_130444.3:c.4930-162_4930-70del (COL18A1)	NP_569711.2:n.4930-162_4930-70del
NM_130445.4:c.3685-162_3685-70del (COL18A1)	NP_569712.2:n.3685-162_3685-70del
NM_001379500.1:c.3694-162_3694-70del (COL18A1) MANE Select	NP_001366429.1:n.3694-162_3694-70del