Canonical Allele Identifier: CA1315428557
Gene: COL5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189058916_189058917delinsTA , CM000664.2:g.189058916_189058917delinsTA GRCh38
NC_000002.11:g.189923642_189923643delinsTA , CM000664.1:g.189923642_189923643delinsTA GRCh37
NC_000002.10:g.189631887_189631888delinsTA NCBI36
NG_011799.1:g.125963_125964delinsTA
NG_011799.2:g.125963_125964delinsTA
NG_011799.3:g.171385_171386delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000374866.9:c.2086-24_2086-23delinsTA MANE Select ENSP00000364000.3:n.2086-24_2086-23delinsTA
ENST00000374866.7:c.2086-24_2086-23delinsTA ENSP00000364000.3:n.2086-24_2086-23delinsTA
ENST00000470524.2:n.192-24_192-23delinsTA
ENST00000618828.1:c.925-24_925-23delinsTA ENSP00000482184.1:n.925-24_925-23delinsTA
NM_000393.3:c.2086-24_2086-23delinsTA NP_000384.2:n.2086-24_2086-23delinsTA
XM_011510573.1:c.1948-24_1948-23delinsTA XP_011508875.1:n.1948-24_1948-23delinsTA
NM_000393.4:c.2086-24_2086-23delinsTA NP_000384.2:n.2086-24_2086-23delinsTA
XM_011510573.3:c.1948-24_1948-23delinsTA XP_011508875.1:n.1948-24_1948-23delinsTA
NM_000393.5:c.2086-24_2086-23delinsTA MANE Select NP_000384.2:n.2086-24_2086-23delinsTA