Canonical Allele Identifier: CA375219600

Gene: HMCN2

Linked Data

• MyVariant Identifiers: chr9:g.133308853G>C (hg19) ; chr9:g.130433466G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433466G>C , CM000671.2:g.130433466G>C	GRCh38
NC_000009.11:g.133308853G>C , CM000671.1:g.133308853G>C	GRCh37
NC_000009.10:g.132298674G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14956G>C	ENSP00000485357.2:p.Ala4986Pro
ENST00000683500.2:c.15013G>C MANE Select	ENSP00000508292.2:p.Ala5005Pro
ENST00000623487.1:n.3359G>C
ENST00000624552.3:c.14953G>C	ENSP00000485357.1:p.Ala4985Pro
NM_001291815.1:c.15013G>C	NP_001278744.1:p.Ala5005Pro
XM_011518465.1:c.14890G>C	XP_011516767.1:p.Ala4964Pro
XM_011518466.1:c.14881G>C	XP_011516768.1:p.Ala4961Pro
XM_011518467.1:c.14836G>C	XP_011516769.1:p.Ala4946Pro
NM_001291815.2:c.15013G>C MANE Select	NP_001278744.1:p.Ala5005Pro
XM_011518465.2:c.14890G>C	XP_011516767.1:p.Ala4964Pro
XM_011518466.2:c.14881G>C	XP_011516768.1:p.Ala4961Pro
XM_011518467.2:c.14836G>C	XP_011516769.1:p.Ala4946Pro
XM_017014585.1:c.11794G>C	XP_016870074.1:p.Ala3932Pro
XM_017014586.1:c.7591G>C	XP_016870075.1:p.Ala2531Pro
XR_001746957.1:n.92+155C>G
XR_001746958.1:n.92+155C>G