Canonical Allele Identifier: CA1881265954

Gene: HMCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433224_130433227delinsGAGA , CM000671.2:g.130433224_130433227delinsGAGA	GRCh38
NC_000009.11:g.133308611_133308614delinsGAGA , CM000671.1:g.133308611_133308614delinsGAGA	GRCh37
NC_000009.10:g.132298432_132298435delinsGAGA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14838-124_14838-121delinsGAGA	ENSP00000485357.2:n.14838-124_14838-121delinsGAGA
ENST00000683500.2:c.14895-124_14895-121delinsGAGA MANE Select	ENSP00000508292.2:n.14895-124_14895-121delinsGAGA
ENST00000623487.1:n.3117_3120delinsGAGA
ENST00000624552.3:c.14835-124_14835-121delinsGAGA	ENSP00000485357.1:n.14835-124_14835-121delinsGAGA
NM_001291815.1:c.14895-124_14895-121delinsGAGA	NP_001278744.1:n.14895-124_14895-121delinsGAGA
XM_011518465.1:c.14772-124_14772-121delinsGAGA	XP_011516767.1:n.14772-124_14772-121delinsGAGA
XM_011518466.1:c.14763-124_14763-121delinsGAGA	XP_011516768.1:n.14763-124_14763-121delinsGAGA
XM_011518467.1:c.14718-124_14718-121delinsGAGA	XP_011516769.1:n.14718-124_14718-121delinsGAGA
NM_001291815.2:c.14895-124_14895-121delinsGAGA MANE Select	NP_001278744.1:n.14895-124_14895-121delinsGAGA
XM_011518465.2:c.14772-124_14772-121delinsGAGA	XP_011516767.1:n.14772-124_14772-121delinsGAGA
XM_011518466.2:c.14763-124_14763-121delinsGAGA	XP_011516768.1:n.14763-124_14763-121delinsGAGA
XM_011518467.2:c.14718-124_14718-121delinsGAGA	XP_011516769.1:n.14718-124_14718-121delinsGAGA
XM_017014585.1:c.11676-124_11676-121delinsGAGA	XP_016870074.1:n.11676-124_11676-121delinsGAGA
XM_017014586.1:c.7473-124_7473-121delinsGAGA	XP_016870075.1:n.7473-124_7473-121delinsGAGA
XR_001746957.1:n.92+394_92+397delinsTCTC
XR_001746958.1:n.92+394_92+397delinsTCTC