Canonical Allele Identifier: CA2692135165

Gene: HMCN2

Linked Data

• gnomAD v4: 9-130433142-TGGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433143_130433145del , CM000671.2:g.130433143_130433145del	GRCh38
NC_000009.11:g.133308530_133308532del , CM000671.1:g.133308530_133308532del	GRCh37
NC_000009.10:g.132298351_132298353del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14838-205_14838-203del	ENSP00000485357.2:n.14838-205_14838-203del
ENST00000683500.2:c.14895-205_14895-203del MANE Select	ENSP00000508292.2:n.14895-205_14895-203del
ENST00000623487.1:n.3036_3038del
ENST00000624552.3:c.14835-205_14835-203del	ENSP00000485357.1:n.14835-205_14835-203del
NM_001291815.1:c.14895-205_14895-203del	NP_001278744.1:n.14895-205_14895-203del
XM_011518465.1:c.14772-205_14772-203del	XP_011516767.1:n.14772-205_14772-203del
XM_011518466.1:c.14763-205_14763-203del	XP_011516768.1:n.14763-205_14763-203del
XM_011518467.1:c.14718-205_14718-203del	XP_011516769.1:n.14718-205_14718-203del
NM_001291815.2:c.14895-205_14895-203del MANE Select	NP_001278744.1:n.14895-205_14895-203del
XM_011518465.2:c.14772-205_14772-203del	XP_011516767.1:n.14772-205_14772-203del
XM_011518466.2:c.14763-205_14763-203del	XP_011516768.1:n.14763-205_14763-203del
XM_011518467.2:c.14718-205_14718-203del	XP_011516769.1:n.14718-205_14718-203del
XM_017014585.1:c.11676-205_11676-203del	XP_016870074.1:n.11676-205_11676-203del
XM_017014586.1:c.7473-205_7473-203del	XP_016870075.1:n.7473-205_7473-203del
XR_001746957.1:n.92+476_92+478del
XR_001746958.1:n.92+476_92+478del