Canonical Allele Identifier: CA2118732781
Gene: COL4A1 HGNC NCBI

Linked Data

dbSNP Id: rs1878030272

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.110179205T>G , CM000675.2:g.110179205T>G GRCh38
NC_000013.10:g.110831552T>G , CM000675.1:g.110831552T>G GRCh37
NC_000013.9:g.109629553T>G NCBI36
NG_011544.2:g.132945A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375820.10:c.2344+66A>C MANE Select ENSP00000364979.4:n.2344+66A>C
ENST00000649738.1:n.2474+66A>C
ENST00000375820.8:c.2344+66A>C ENSP00000364979.4:n.2344+66A>C
NM_001845.5:c.2344+66A>C NP_001836.3:n.2344+66A>C
XM_011521048.1:c.2152+66A>C XP_011519350.1:n.2152+66A>C
XM_011521048.2:c.2152+66A>C XP_011519350.1:n.2152+66A>C
NM_001845.6:c.2344+66A>C MANE Select NP_001836.3:n.2344+66A>C