Canonical Allele Identifier: CA1315428681
Gene: COL5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189059243A= , CM000664.2:g.189059243A= GRCh38
NC_000002.11:g.189923969A= , CM000664.1:g.189923969A= GRCh37
NC_000002.10:g.189632214A= NCBI36
NG_011799.1:g.125637T=
NG_011799.2:g.125637T=
NG_011799.3:g.171059T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374866.9:c.2086-350T= MANE Select ENSP00000364000.3:n.2086-350T=
ENST00000374866.7:c.2086-350T= ENSP00000364000.3:n.2086-350T=
ENST00000470524.2:n.192-350T=
ENST00000618828.1:c.925-350T= ENSP00000482184.1:n.925-350T=
NM_000393.3:c.2086-350T= NP_000384.2:n.2086-350T=
XM_011510573.1:c.1948-350T= XP_011508875.1:n.1948-350T=
NM_000393.4:c.2086-350T= NP_000384.2:n.2086-350T=
XM_011510573.3:c.1948-350T= XP_011508875.1:n.1948-350T=
NM_000393.5:c.2086-350T= MANE Select NP_000384.2:n.2086-350T=