Canonical Allele Identifier: CA2692135408

Gene: HMCN2

Linked Data

• gnomAD v4: 9-130433273-T-TTTTA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433273_130433274insTTTA , CM000671.2:g.130433273_130433274insTTTA	GRCh38
NC_000009.11:g.133308660_133308661insTTTA , CM000671.1:g.133308660_133308661insTTTA	GRCh37
NC_000009.10:g.132298481_132298482insTTTA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14838-75_14838-74insTTTA	ENSP00000485357.2:n.14838-75_14838-74insTTTA
ENST00000683500.2:c.14895-75_14895-74insTTTA MANE Select	ENSP00000508292.2:n.14895-75_14895-74insTTTA
ENST00000623487.1:n.3166_3167insTTTA
ENST00000624552.3:c.14835-75_14835-74insTTTA	ENSP00000485357.1:n.14835-75_14835-74insTTTA
NM_001291815.1:c.14895-75_14895-74insTTTA	NP_001278744.1:n.14895-75_14895-74insTTTA
XM_011518465.1:c.14772-75_14772-74insTTTA	XP_011516767.1:n.14772-75_14772-74insTTTA
XM_011518466.1:c.14763-75_14763-74insTTTA	XP_011516768.1:n.14763-75_14763-74insTTTA
XM_011518467.1:c.14718-75_14718-74insTTTA	XP_011516769.1:n.14718-75_14718-74insTTTA
NM_001291815.2:c.14895-75_14895-74insTTTA MANE Select	NP_001278744.1:n.14895-75_14895-74insTTTA
XM_011518465.2:c.14772-75_14772-74insTTTA	XP_011516767.1:n.14772-75_14772-74insTTTA
XM_011518466.2:c.14763-75_14763-74insTTTA	XP_011516768.1:n.14763-75_14763-74insTTTA
XM_011518467.2:c.14718-75_14718-74insTTTA	XP_011516769.1:n.14718-75_14718-74insTTTA
XM_017014585.1:c.11676-75_11676-74insTTTA	XP_016870074.1:n.11676-75_11676-74insTTTA
XM_017014586.1:c.7473-75_7473-74insTTTA	XP_016870075.1:n.7473-75_7473-74insTTTA
XR_001746957.1:n.92+347_92+348insTAAA
XR_001746958.1:n.92+347_92+348insTAAA