Canonical Allele Identifier: CA484789114
Gene: COL4A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.110826266T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.110173919T>A , CM000675.2:g.110173919T>A GRCh38
NC_000013.10:g.110826266T>A , CM000675.1:g.110826266T>A GRCh37
NC_000013.9:g.109624267T>A NCBI36
NG_011544.2:g.138231A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000375820.10:c.3486A>T MANE Select ENSP00000364979.4:p.Ala1162=
ENST00000375820.8:c.3486A>T ENSP00000364979.4:p.Ala1162=
NM_001845.5:c.3486A>T NP_001836.3:p.Ala1162=
XM_011521048.1:c.3294A>T XP_011519350.1:p.Ala1098=
XM_011521048.2:c.3294A>T XP_011519350.1:p.Ala1098=
NM_001845.6:c.3486A>T MANE Select NP_001836.3:p.Ala1162=