Canonical Allele Identifier: CA1315445918
Gene: COL5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189098757T= , CM000664.2:g.189098757T= GRCh38
NC_000002.11:g.189963483T= , CM000664.1:g.189963483T= GRCh37
NC_000002.10:g.189671728T= NCBI36
NG_011799.1:g.86123A=
NG_011799.2:g.86123A=
NG_011799.3:g.131545A=

Transcript Alleles

HGVS Amino-acid change
ENST00000374866.9:c.372A= MANE Select ENSP00000364000.3:p.Val124=
ENST00000649966.1:c.234A= ENSP00000496785.1:p.Val78=
ENST00000374866.7:c.372A= ENSP00000364000.3:p.Val124=
ENST00000618828.1:c.-259A= ENSP00000482184.1:n.-259A=
NM_000393.3:c.372A= NP_000384.2:p.Val124=
XM_011510573.1:c.234A= XP_011508875.1:p.Val78=
NM_000393.4:c.372A= NP_000384.2:p.Val124=
XM_011510573.3:c.234A= XP_011508875.1:p.Val78=
NM_000393.5:c.372A= MANE Select NP_000384.2:p.Val124=