Canonical Allele Identifier: CA349854992
Gene: COL5A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189035016T>C , CM000664.2:g.189035016T>C GRCh38
NC_000002.11:g.189899742T>C , CM000664.1:g.189899742T>C GRCh37
NC_000002.10:g.189607987T>C NCBI36
NG_011799.1:g.149864A>G
NG_011799.2:g.149864A>G
NG_011799.3:g.195286A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000374866.9:c.4253A>G MANE Select ENSP00000364000.3:p.Asn1418Ser
ENST00000374866.7:c.4253A>G ENSP00000364000.3:p.Asn1418Ser
ENST00000618828.1:c.3092A>G ENSP00000482184.1:p.Asn1031Ser
NM_000393.3:c.4253A>G NP_000384.2:p.Asn1418Ser
XM_011510573.1:c.4115A>G XP_011508875.1:p.Asn1372Ser
NM_000393.4:c.4253A>G NP_000384.2:p.Asn1418Ser
XM_011510573.3:c.4115A>G XP_011508875.1:p.Asn1372Ser
NM_000393.5:c.4253A>G MANE Select NP_000384.2:p.Asn1418Ser