Canonical Allele Identifier: CA410514384

Gene: COL18A1

Linked Data

• MyVariant Identifiers: chr21:g.46896310A>T (hg19) ; chr21:g.45476396A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.45476396A>T , CM000683.2:g.45476396A>T	GRCh38
NC_000021.8:g.46896310A>T , CM000683.1:g.46896310A>T	GRCh37
NC_000021.7:g.45720738A>T	NCBI36
NG_011903.1:g.76214A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355480.10:c.1384A>T	ENSP00000347665.5:p.Thr462Ser
ENST00000651438.1:c.844A>T MANE Select	ENSP00000498485.1:p.Thr282Ser
ENST00000355480.9:c.1384A>T	ENSP00000347665.5:p.Thr462Ser
ENST00000359759.8:c.2089A>T	ENSP00000352798.4:p.Thr697Ser
ENST00000400337.6:c.844A>T	ENSP00000383191.2:p.Thr282Ser
NM_030582.3:c.1384A>T	NP_085059.2:p.Thr462Ser
NM_130444.2:c.2089A>T	NP_569711.2:p.Thr697Ser
NM_130445.3:c.844A>T	NP_569712.2:p.Thr282Ser
NM_030582.4:c.1384A>T	NP_085059.2:p.Thr462Ser
NM_130444.3:c.2089A>T	NP_569711.2:p.Thr697Ser
NM_130445.4:c.844A>T	NP_569712.2:p.Thr282Ser
NM_001379500.1:c.844A>T MANE Select	NP_001366429.1:p.Thr282Ser