Canonical Allele Identifier: CA1881265724

Gene: HMCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130432951_130432952delinsCG , CM000671.2:g.130432951_130432952delinsCG	GRCh38
NC_000009.11:g.133308338_133308339delinsCG , CM000671.1:g.133308338_133308339delinsCG	GRCh37
NC_000009.10:g.132298159_132298160delinsCG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14838-397_14838-396delinsCG	ENSP00000485357.2:n.14838-397_14838-396delinsCG
ENST00000683500.2:c.14895-397_14895-396delinsCG MANE Select	ENSP00000508292.2:n.14895-397_14895-396delinsCG
ENST00000623487.1:n.2844_2845delinsCG
ENST00000624552.3:c.14835-397_14835-396delinsCG	ENSP00000485357.1:n.14835-397_14835-396delinsCG
NM_001291815.1:c.14895-397_14895-396delinsCG	NP_001278744.1:n.14895-397_14895-396delinsCG
XM_011518465.1:c.14772-397_14772-396delinsCG	XP_011516767.1:n.14772-397_14772-396delinsCG
XM_011518466.1:c.14763-397_14763-396delinsCG	XP_011516768.1:n.14763-397_14763-396delinsCG
XM_011518467.1:c.14718-397_14718-396delinsCG	XP_011516769.1:n.14718-397_14718-396delinsCG
NM_001291815.2:c.14895-397_14895-396delinsCG MANE Select	NP_001278744.1:n.14895-397_14895-396delinsCG
XM_011518465.2:c.14772-397_14772-396delinsCG	XP_011516767.1:n.14772-397_14772-396delinsCG
XM_011518466.2:c.14763-397_14763-396delinsCG	XP_011516768.1:n.14763-397_14763-396delinsCG
XM_011518467.2:c.14718-397_14718-396delinsCG	XP_011516769.1:n.14718-397_14718-396delinsCG
XM_017014585.1:c.11676-397_11676-396delinsCG	XP_016870074.1:n.11676-397_11676-396delinsCG
XM_017014586.1:c.7473-397_7473-396delinsCG	XP_016870075.1:n.7473-397_7473-396delinsCG
XR_001746957.1:n.92+669_92+670delinsCG
XR_001746958.1:n.92+669_92+670delinsCG