Canonical Allele Identifier: CA2692135590

Gene: HMCN2

Linked Data

• gnomAD v4: 9-130433434-TGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433439_130433440del , CM000671.2:g.130433439_130433440del	GRCh38
NC_000009.11:g.133308826_133308827del , CM000671.1:g.133308826_133308827del	GRCh37
NC_000009.10:g.132298647_132298648del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14929_14930del	ENSP00000485357.2:p.Ala4977ProfsTer?
ENST00000683500.2:c.14986_14987del MANE Select	ENSP00000508292.2:p.Ala4996ProfsTer?
ENST00000623487.1:n.3332_3333del
ENST00000624552.3:c.14926_14927del	ENSP00000485357.1:p.Ala4976ProfsTer?
NM_001291815.1:c.14986_14987del	NP_001278744.1:p.Ala4996ProfsTer?
XM_011518465.1:c.14863_14864del	XP_011516767.1:p.Ala4955ProfsTer?
XM_011518466.1:c.14854_14855del	XP_011516768.1:p.Ala4952ProfsTer?
XM_011518467.1:c.14809_14810del	XP_011516769.1:p.Ala4937ProfsTer?
NM_001291815.2:c.14986_14987del MANE Select	NP_001278744.1:p.Ala4996ProfsTer?
XM_011518465.2:c.14863_14864del	XP_011516767.1:p.Ala4955ProfsTer?
XM_011518466.2:c.14854_14855del	XP_011516768.1:p.Ala4952ProfsTer?
XM_011518467.2:c.14809_14810del	XP_011516769.1:p.Ala4937ProfsTer?
XM_017014585.1:c.11767_11768del	XP_016870074.1:p.Ala3923ProfsTer?
XM_017014586.1:c.7564_7565del	XP_016870075.1:p.Ala2522ProfsTer?
XR_001746957.1:n.92+185_92+186del
XR_001746958.1:n.92+185_92+186del