Canonical Allele Identifier: CA1881266234
Gene: HMCN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130433393C= , CM000671.2:g.130433393C= GRCh38
NC_000009.11:g.133308780C= , CM000671.1:g.133308780C= GRCh37
NC_000009.10:g.132298601C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000624552.4:c.14883C= ENSP00000485357.2:p.Pro4961=
ENST00000683500.2:c.14940C= MANE Select ENSP00000508292.2:p.Pro4980=
ENST00000623487.1:n.3286C=
ENST00000624552.3:c.14880C= ENSP00000485357.1:p.Pro4960=
NM_001291815.1:c.14940C= NP_001278744.1:p.Pro4980=
XM_011518465.1:c.14817C= XP_011516767.1:p.Pro4939=
XM_011518466.1:c.14808C= XP_011516768.1:p.Pro4936=
XM_011518467.1:c.14763C= XP_011516769.1:p.Pro4921=
NM_001291815.2:c.14940C= MANE Select NP_001278744.1:p.Pro4980=
XM_011518465.2:c.14817C= XP_011516767.1:p.Pro4939=
XM_011518466.2:c.14808C= XP_011516768.1:p.Pro4936=
XM_011518467.2:c.14763C= XP_011516769.1:p.Pro4921=
XM_017014585.1:c.11721C= XP_016870074.1:p.Pro3907=
XM_017014586.1:c.7518C= XP_016870075.1:p.Pro2506=
XR_001746957.1:n.92+228G=
XR_001746958.1:n.92+228G=