Canonical Allele Identifier: CA2692135232

Gene: HMCN2

Linked Data

• gnomAD v4: 9-130433186-CGTGGGA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433188_130433193del , CM000671.2:g.130433188_130433193del	GRCh38
NC_000009.11:g.133308575_133308580del , CM000671.1:g.133308575_133308580del	GRCh37
NC_000009.10:g.132298396_132298401del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14838-160_14838-155del	ENSP00000485357.2:n.14838-160_14838-155del
ENST00000683500.2:c.14895-160_14895-155del MANE Select	ENSP00000508292.2:n.14895-160_14895-155del
ENST00000623487.1:n.3081_3086del
ENST00000624552.3:c.14835-160_14835-155del	ENSP00000485357.1:n.14835-160_14835-155del
NM_001291815.1:c.14895-160_14895-155del	NP_001278744.1:n.14895-160_14895-155del
XM_011518465.1:c.14772-160_14772-155del	XP_011516767.1:n.14772-160_14772-155del
XM_011518466.1:c.14763-160_14763-155del	XP_011516768.1:n.14763-160_14763-155del
XM_011518467.1:c.14718-160_14718-155del	XP_011516769.1:n.14718-160_14718-155del
NM_001291815.2:c.14895-160_14895-155del MANE Select	NP_001278744.1:n.14895-160_14895-155del
XM_011518465.2:c.14772-160_14772-155del	XP_011516767.1:n.14772-160_14772-155del
XM_011518466.2:c.14763-160_14763-155del	XP_011516768.1:n.14763-160_14763-155del
XM_011518467.2:c.14718-160_14718-155del	XP_011516769.1:n.14718-160_14718-155del
XM_017014585.1:c.11676-160_11676-155del	XP_016870074.1:n.11676-160_11676-155del
XM_017014586.1:c.7473-160_7473-155del	XP_016870075.1:n.7473-160_7473-155del
XR_001746957.1:n.92+429_92+434del
XR_001746958.1:n.92+429_92+434del