Canonical Allele Identifier: CA349863972
Gene: COL5A2 HGNC NCBI

Linked Data

dbSNP Id: rs1686973835
COSMIC: COSM310263

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189098755G>T , CM000664.2:g.189098755G>T GRCh38
NC_000002.11:g.189963481G>T , CM000664.1:g.189963481G>T GRCh37
NC_000002.10:g.189671726G>T NCBI36
NG_011799.1:g.86125C>A
NG_011799.2:g.86125C>A
NG_011799.3:g.131547C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000374866.9:c.374C>A MANE Select ENSP00000364000.3:p.Thr125Lys
ENST00000649966.1:c.236C>A ENSP00000496785.1:p.Thr79Lys
ENST00000374866.7:c.374C>A ENSP00000364000.3:p.Thr125Lys
ENST00000618828.1:c.-257C>A ENSP00000482184.1:n.-257C>A
NM_000393.3:c.374C>A NP_000384.2:p.Thr125Lys
XM_011510573.1:c.236C>A XP_011508875.1:p.Thr79Lys
NM_000393.4:c.374C>A NP_000384.2:p.Thr125Lys
XM_011510573.3:c.236C>A XP_011508875.1:p.Thr79Lys
NM_000393.5:c.374C>A MANE Select NP_000384.2:p.Thr125Lys