Canonical Allele Identifier: CA388661887
Gene: COL4A1 HGNC NCBI

Linked Data

dbSNP Id: rs1877517501

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.110169711T>G , CM000675.2:g.110169711T>G GRCh38
NC_000013.10:g.110822058T>G , CM000675.1:g.110822058T>G GRCh37
NC_000013.9:g.109620059T>G NCBI36
NG_011544.2:g.142439A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000375820.10:c.3794A>C MANE Select ENSP00000364979.4:p.Lys1265Thr
ENST00000375820.8:c.3794A>C ENSP00000364979.4:p.Lys1265Thr
NM_001845.5:c.3794A>C NP_001836.3:p.Lys1265Thr
XM_011521048.1:c.3602A>C XP_011519350.1:p.Lys1201Thr
XM_011521048.2:c.3602A>C XP_011519350.1:p.Lys1201Thr
NM_001845.6:c.3794A>C MANE Select NP_001836.3:p.Lys1265Thr