Canonical Allele Identifier: CA2692134942

Gene: HMCN2

Linked Data

• gnomAD v4: 9-130432984-A-AGC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130432984_130432985insGC , CM000671.2:g.130432984_130432985insGC	GRCh38
NC_000009.11:g.133308371_133308372insGC , CM000671.1:g.133308371_133308372insGC	GRCh37
NC_000009.10:g.132298192_132298193insGC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14838-364_14838-363insGC	ENSP00000485357.2:n.14838-364_14838-363insGC
ENST00000683500.2:c.14895-364_14895-363insGC MANE Select	ENSP00000508292.2:n.14895-364_14895-363insGC
ENST00000623487.1:n.2877_2878insGC
ENST00000624552.3:c.14835-364_14835-363insGC	ENSP00000485357.1:n.14835-364_14835-363insGC
NM_001291815.1:c.14895-364_14895-363insGC	NP_001278744.1:n.14895-364_14895-363insGC
XM_011518465.1:c.14772-364_14772-363insGC	XP_011516767.1:n.14772-364_14772-363insGC
XM_011518466.1:c.14763-364_14763-363insGC	XP_011516768.1:n.14763-364_14763-363insGC
XM_011518467.1:c.14718-364_14718-363insGC	XP_011516769.1:n.14718-364_14718-363insGC
NM_001291815.2:c.14895-364_14895-363insGC MANE Select	NP_001278744.1:n.14895-364_14895-363insGC
XM_011518465.2:c.14772-364_14772-363insGC	XP_011516767.1:n.14772-364_14772-363insGC
XM_011518466.2:c.14763-364_14763-363insGC	XP_011516768.1:n.14763-364_14763-363insGC
XM_011518467.2:c.14718-364_14718-363insGC	XP_011516769.1:n.14718-364_14718-363insGC
XM_017014585.1:c.11676-364_11676-363insGC	XP_016870074.1:n.11676-364_11676-363insGC
XM_017014586.1:c.7473-364_7473-363insGC	XP_016870075.1:n.7473-364_7473-363insGC
XR_001746957.1:n.92+636_92+637insGC
XR_001746958.1:n.92+636_92+637insGC