Canonical Allele Identifier: CA1881266054

Gene: HMCN2

Linked Data

• dbSNP Id: rs1844871587

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433293_130433295del , CM000671.2:g.130433293_130433295del	GRCh38
NC_000009.11:g.133308680_133308682del , CM000671.1:g.133308680_133308682del	GRCh37
NC_000009.10:g.132298501_132298503del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14838-55_14838-53del	ENSP00000485357.2:n.14838-55_14838-53del
ENST00000683500.2:c.14895-55_14895-53del MANE Select	ENSP00000508292.2:n.14895-55_14895-53del
ENST00000623487.1:n.3186_3188del
ENST00000624552.3:c.14835-55_14835-53del	ENSP00000485357.1:n.14835-55_14835-53del
NM_001291815.1:c.14895-55_14895-53del	NP_001278744.1:n.14895-55_14895-53del
XM_011518465.1:c.14772-55_14772-53del	XP_011516767.1:n.14772-55_14772-53del
XM_011518466.1:c.14763-55_14763-53del	XP_011516768.1:n.14763-55_14763-53del
XM_011518467.1:c.14718-55_14718-53del	XP_011516769.1:n.14718-55_14718-53del
NM_001291815.2:c.14895-55_14895-53del MANE Select	NP_001278744.1:n.14895-55_14895-53del
XM_011518465.2:c.14772-55_14772-53del	XP_011516767.1:n.14772-55_14772-53del
XM_011518466.2:c.14763-55_14763-53del	XP_011516768.1:n.14763-55_14763-53del
XM_011518467.2:c.14718-55_14718-53del	XP_011516769.1:n.14718-55_14718-53del
XM_017014585.1:c.11676-55_11676-53del	XP_016870074.1:n.11676-55_11676-53del
XM_017014586.1:c.7473-55_7473-53del	XP_016870075.1:n.7473-55_7473-53del
XR_001746957.1:n.92+327_92+329del
XR_001746958.1:n.92+327_92+329del