Canonical Allele Identifier: CA484788766
Gene: COL4A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.110822057T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.110169710T>C , CM000675.2:g.110169710T>C GRCh38
NC_000013.10:g.110822057T>C , CM000675.1:g.110822057T>C GRCh37
NC_000013.9:g.109620058T>C NCBI36
NG_011544.2:g.142440A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000375820.10:c.3795A>G MANE Select ENSP00000364979.4:p.Lys1265=
ENST00000375820.8:c.3795A>G ENSP00000364979.4:p.Lys1265=
NM_001845.5:c.3795A>G NP_001836.3:p.Lys1265=
XM_011521048.1:c.3603A>G XP_011519350.1:p.Lys1201=
XM_011521048.2:c.3603A>G XP_011519350.1:p.Lys1201=
NM_001845.6:c.3795A>G MANE Select NP_001836.3:p.Lys1265=