Canonical Allele Identifier: CA2692135005

Gene: HMCN2

Linked Data

• gnomAD v4: 9-130433035-GACT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433036_130433038del , CM000671.2:g.130433036_130433038del	GRCh38
NC_000009.11:g.133308423_133308425del , CM000671.1:g.133308423_133308425del	GRCh37
NC_000009.10:g.132298244_132298246del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14838-312_14838-310del	ENSP00000485357.2:n.14838-312_14838-310del
ENST00000683500.2:c.14895-312_14895-310del MANE Select	ENSP00000508292.2:n.14895-312_14895-310del
ENST00000623487.1:n.2929_2931del
ENST00000624552.3:c.14835-312_14835-310del	ENSP00000485357.1:n.14835-312_14835-310del
NM_001291815.1:c.14895-312_14895-310del	NP_001278744.1:n.14895-312_14895-310del
XM_011518465.1:c.14772-312_14772-310del	XP_011516767.1:n.14772-312_14772-310del
XM_011518466.1:c.14763-312_14763-310del	XP_011516768.1:n.14763-312_14763-310del
XM_011518467.1:c.14718-312_14718-310del	XP_011516769.1:n.14718-312_14718-310del
NM_001291815.2:c.14895-312_14895-310del MANE Select	NP_001278744.1:n.14895-312_14895-310del
XM_011518465.2:c.14772-312_14772-310del	XP_011516767.1:n.14772-312_14772-310del
XM_011518466.2:c.14763-312_14763-310del	XP_011516768.1:n.14763-312_14763-310del
XM_011518467.2:c.14718-312_14718-310del	XP_011516769.1:n.14718-312_14718-310del
XM_017014585.1:c.11676-312_11676-310del	XP_016870074.1:n.11676-312_11676-310del
XM_017014586.1:c.7473-312_7473-310del	XP_016870075.1:n.7473-312_7473-310del
XR_001746957.1:n.92+583_92+585del
XR_001746958.1:n.92+583_92+585del