Canonical Allele Identifier: CA430324422
Gene: COL5A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.189927630T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189062904T>C , CM000664.2:g.189062904T>C GRCh38
NC_000002.11:g.189927630T>C , CM000664.1:g.189927630T>C GRCh37
NC_000002.10:g.189635875T>C NCBI36
NG_011799.1:g.121976A>G
NG_011799.2:g.121976A>G
NG_011799.3:g.167398A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000374866.9:c.1938A>G MANE Select ENSP00000364000.3:p.Lys646=
ENST00000374866.7:c.1938A>G ENSP00000364000.3:p.Lys646=
ENST00000470524.2:n.44A>G
ENST00000618828.1:c.777A>G ENSP00000482184.1:p.Lys259=
NM_000393.3:c.1938A>G NP_000384.2:p.Lys646=
XM_011510573.1:c.1800A>G XP_011508875.1:p.Lys600=
NM_000393.4:c.1938A>G NP_000384.2:p.Lys646=
XM_011510573.3:c.1800A>G XP_011508875.1:p.Lys600=
NM_000393.5:c.1938A>G MANE Select NP_000384.2:p.Lys646=