Canonical Allele Identifier: CA1387934104
Gene: COL8A1 HGNC NCBI

Linked Data

dbSNP Id: rs1938734666

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.99677461A>T , CM000665.2:g.99677461A>T GRCh38
NC_000003.11:g.99396305A>T , CM000665.1:g.99396305A>T GRCh37
NC_000003.10:g.100878995A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000652472.1:c.-129+38797A>T MANE Select ENSP00000498483.1:n.-129+38797A>T
ENST00000261037.7:c.-129+1740A>T ENSP00000261037.3:n.-129+1740A>T
ENST00000273342.8:c.-129+38797A>T ENSP00000273342.3:n.-129+38797A>T
ENST00000452013.5:c.-129+38797A>T ENSP00000387589.1:n.-129+38797A>T
ENST00000463753.5:n.253-290A>T
ENST00000474648.5:n.252+1740A>T
ENST00000483969.5:n.252+1740A>T
ENST00000621757.1:c.-298-13938A>T ENSP00000482679.1:n.-298-13938A>T
NM_001850.4:c.-129+1740A>T NP_001841.2:n.-129+1740A>T
NM_020351.3:c.-129+38797A>T NP_065084.2:n.-129+38797A>T
NM_020351.4:c.-129+38797A>T MANE Select NP_065084.2:n.-129+38797A>T
NM_001850.5:c.-129+1740A>T NP_001841.2:n.-129+1740A>T