Canonical Allele Identifier: CA2692134978

Gene: HMCN2

Linked Data

• gnomAD v4: 9-130433015-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433015_130433016insA , CM000671.2:g.130433015_130433016insA	GRCh38
NC_000009.11:g.133308402_133308403insA , CM000671.1:g.133308402_133308403insA	GRCh37
NC_000009.10:g.132298223_132298224insA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14838-333_14838-332insA	ENSP00000485357.2:n.14838-333_14838-332insA
ENST00000683500.2:c.14895-333_14895-332insA MANE Select	ENSP00000508292.2:n.14895-333_14895-332insA
ENST00000623487.1:n.2908_2909insA
ENST00000624552.3:c.14835-333_14835-332insA	ENSP00000485357.1:n.14835-333_14835-332insA
NM_001291815.1:c.14895-333_14895-332insA	NP_001278744.1:n.14895-333_14895-332insA
XM_011518465.1:c.14772-333_14772-332insA	XP_011516767.1:n.14772-333_14772-332insA
XM_011518466.1:c.14763-333_14763-332insA	XP_011516768.1:n.14763-333_14763-332insA
XM_011518467.1:c.14718-333_14718-332insA	XP_011516769.1:n.14718-333_14718-332insA
NM_001291815.2:c.14895-333_14895-332insA MANE Select	NP_001278744.1:n.14895-333_14895-332insA
XM_011518465.2:c.14772-333_14772-332insA	XP_011516767.1:n.14772-333_14772-332insA
XM_011518466.2:c.14763-333_14763-332insA	XP_011516768.1:n.14763-333_14763-332insA
XM_011518467.2:c.14718-333_14718-332insA	XP_011516769.1:n.14718-333_14718-332insA
XM_017014585.1:c.11676-333_11676-332insA	XP_016870074.1:n.11676-333_11676-332insA
XM_017014586.1:c.7473-333_7473-332insA	XP_016870075.1:n.7473-333_7473-332insA
XR_001746957.1:n.92+605_92+606insT
XR_001746958.1:n.92+605_92+606insT