Canonical Allele Identifier: CA1881266059

Gene: HMCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433294_130433296delinsACG , CM000671.2:g.130433294_130433296delinsACG	GRCh38
NC_000009.11:g.133308681_133308683delinsACG , CM000671.1:g.133308681_133308683delinsACG	GRCh37
NC_000009.10:g.132298502_132298504delinsACG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14838-54_14838-52delinsACG	ENSP00000485357.2:n.14838-54_14838-52delinsACG
ENST00000683500.2:c.14895-54_14895-52delinsACG MANE Select	ENSP00000508292.2:n.14895-54_14895-52delinsACG
ENST00000623487.1:n.3187_3189delinsACG
ENST00000624552.3:c.14835-54_14835-52delinsACG	ENSP00000485357.1:n.14835-54_14835-52delinsACG
NM_001291815.1:c.14895-54_14895-52delinsACG	NP_001278744.1:n.14895-54_14895-52delinsACG
XM_011518465.1:c.14772-54_14772-52delinsACG	XP_011516767.1:n.14772-54_14772-52delinsACG
XM_011518466.1:c.14763-54_14763-52delinsACG	XP_011516768.1:n.14763-54_14763-52delinsACG
XM_011518467.1:c.14718-54_14718-52delinsACG	XP_011516769.1:n.14718-54_14718-52delinsACG
NM_001291815.2:c.14895-54_14895-52delinsACG MANE Select	NP_001278744.1:n.14895-54_14895-52delinsACG
XM_011518465.2:c.14772-54_14772-52delinsACG	XP_011516767.1:n.14772-54_14772-52delinsACG
XM_011518466.2:c.14763-54_14763-52delinsACG	XP_011516768.1:n.14763-54_14763-52delinsACG
XM_011518467.2:c.14718-54_14718-52delinsACG	XP_011516769.1:n.14718-54_14718-52delinsACG
XM_017014585.1:c.11676-54_11676-52delinsACG	XP_016870074.1:n.11676-54_11676-52delinsACG
XM_017014586.1:c.7473-54_7473-52delinsACG	XP_016870075.1:n.7473-54_7473-52delinsACG
XR_001746957.1:n.92+325_92+327delinsCGT
XR_001746958.1:n.92+325_92+327delinsCGT