Canonical Allele Identifier: CA375219624

Gene: HMCN2

Linked Data

• MyVariant Identifiers: chr9:g.133308859T>A (hg19) ; chr9:g.130433472T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433472T>A , CM000671.2:g.130433472T>A	GRCh38
NC_000009.11:g.133308859T>A , CM000671.1:g.133308859T>A	GRCh37
NC_000009.10:g.132298680T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14962T>A	ENSP00000485357.2:p.Ser4988Thr
ENST00000683500.2:c.15019T>A MANE Select	ENSP00000508292.2:p.Ser5007Thr
ENST00000623487.1:n.3365T>A
ENST00000624552.3:c.14959T>A	ENSP00000485357.1:p.Ser4987Thr
NM_001291815.1:c.15019T>A	NP_001278744.1:p.Ser5007Thr
XM_011518465.1:c.14896T>A	XP_011516767.1:p.Ser4966Thr
XM_011518466.1:c.14887T>A	XP_011516768.1:p.Ser4963Thr
XM_011518467.1:c.14842T>A	XP_011516769.1:p.Ser4948Thr
NM_001291815.2:c.15019T>A MANE Select	NP_001278744.1:p.Ser5007Thr
XM_011518465.2:c.14896T>A	XP_011516767.1:p.Ser4966Thr
XM_011518466.2:c.14887T>A	XP_011516768.1:p.Ser4963Thr
XM_011518467.2:c.14842T>A	XP_011516769.1:p.Ser4948Thr
XM_017014585.1:c.11800T>A	XP_016870074.1:p.Ser3934Thr
XM_017014586.1:c.7597T>A	XP_016870075.1:p.Ser2533Thr
XR_001746957.1:n.92+149A>T
XR_001746958.1:n.92+149A>T