Canonical Allele Identifier: CA1881266276

Gene: HMCN2

Linked Data

• dbSNP Id: rs1844885113

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433413_130433418dup , CM000671.2:g.130433413_130433418dup	GRCh38
NC_000009.11:g.133308800_133308805dup , CM000671.1:g.133308800_133308805dup	GRCh37
NC_000009.10:g.132298621_132298626dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14903_14908dup	ENSP00000485357.2:p.Leu4969_Pro4970insLeuLeu
ENST00000683500.2:c.14960_14965dup MANE Select	ENSP00000508292.2:p.Leu4988_Pro4989insLeuLeu
ENST00000623487.1:n.3306_3311dup
ENST00000624552.3:c.14900_14905dup	ENSP00000485357.1:p.Leu4968_Pro4969insLeuLeu
NM_001291815.1:c.14960_14965dup	NP_001278744.1:p.Leu4988_Pro4989insLeuLeu
XM_011518465.1:c.14837_14842dup	XP_011516767.1:p.Leu4947_Pro4948insLeuLeu
XM_011518466.1:c.14828_14833dup	XP_011516768.1:p.Leu4944_Pro4945insLeuLeu
XM_011518467.1:c.14783_14788dup	XP_011516769.1:p.Leu4929_Pro4930insLeuLeu
NM_001291815.2:c.14960_14965dup MANE Select	NP_001278744.1:p.Leu4988_Pro4989insLeuLeu
XM_011518465.2:c.14837_14842dup	XP_011516767.1:p.Leu4947_Pro4948insLeuLeu
XM_011518466.2:c.14828_14833dup	XP_011516768.1:p.Leu4944_Pro4945insLeuLeu
XM_011518467.2:c.14783_14788dup	XP_011516769.1:p.Leu4929_Pro4930insLeuLeu
XM_017014585.1:c.11741_11746dup	XP_016870074.1:p.Leu3915_Pro3916insLeuLeu
XM_017014586.1:c.7538_7543dup	XP_016870075.1:p.Leu2514_Pro2515insLeuLeu
XR_001746957.1:n.92+205_92+210dup
XR_001746958.1:n.92+205_92+210dup