Canonical Allele Identifier: CA2786081113

Gene: HMCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433080_130433087del , CM000671.2:g.130433080_130433087del	GRCh38
NC_000009.11:g.133308467_133308474del , CM000671.1:g.133308467_133308474del	GRCh37
NC_000009.10:g.132298288_132298295del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14838-268_14838-261del	ENSP00000485357.2:n.14838-268_14838-261del
ENST00000683500.2:c.14895-268_14895-261del MANE Select	ENSP00000508292.2:n.14895-268_14895-261del
ENST00000623487.1:n.2973_2980del
ENST00000624552.3:c.14835-268_14835-261del	ENSP00000485357.1:n.14835-268_14835-261del
NM_001291815.1:c.14895-268_14895-261del	NP_001278744.1:n.14895-268_14895-261del
XM_011518465.1:c.14772-268_14772-261del	XP_011516767.1:n.14772-268_14772-261del
XM_011518466.1:c.14763-268_14763-261del	XP_011516768.1:n.14763-268_14763-261del
XM_011518467.1:c.14718-268_14718-261del	XP_011516769.1:n.14718-268_14718-261del
NM_001291815.2:c.14895-268_14895-261del MANE Select	NP_001278744.1:n.14895-268_14895-261del
XM_011518465.2:c.14772-268_14772-261del	XP_011516767.1:n.14772-268_14772-261del
XM_011518466.2:c.14763-268_14763-261del	XP_011516768.1:n.14763-268_14763-261del
XM_011518467.2:c.14718-268_14718-261del	XP_011516769.1:n.14718-268_14718-261del
XM_017014585.1:c.11676-268_11676-261del	XP_016870074.1:n.11676-268_11676-261del
XM_017014586.1:c.7473-268_7473-261del	XP_016870075.1:n.7473-268_7473-261del
XR_001746957.1:n.92+535_92+542del
XR_001746958.1:n.92+535_92+542del