Canonical Allele Identifier: CA2691805867

Gene: ENG

Linked Data

• gnomAD v4: 9-127816084-A-ACTCTGC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127816086_127816091dup , CM000671.2:g.127816086_127816091dup	GRCh38
NC_000009.11:g.130578365_130578370dup , CM000671.1:g.130578365_130578370dup	GRCh37
NC_000009.10:g.129618186_129618191dup	NCBI36
NG_009551.1:g.43679_43684dup , LRG_589:g.43679_43684dup
NG_023245.1:g.18212_18217dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.1196-37_1196-32dup	ENSP00000479015.1:n.1196-37_1196-32dup
ENST00000373203.9:c.1742-37_1742-32dup MANE Select	ENSP00000362299.4:n.1742-37_1742-32dup
ENST00000344849.4:c.1742-37_1742-32dup	ENSP00000341917.3:n.1742-37_1742-32dup
ENST00000373203.8:c.1742-37_1742-32dup	ENSP00000362299.4:n.1742-37_1742-32dup
ENST00000480266.5:c.1196-37_1196-32dup	ENSP00000479015.1:n.1196-37_1196-32dup
NM_000118.3:c.1742-37_1742-32dup , LRG_589t1:c.1742-37_1742-32dup	NP_000109.1:n.1742-37_1742-32dup
NM_001114753.2:c.1742-37_1742-32dup , LRG_589t2:c.1742-37_1742-32dup	NP_001108225.1:n.1742-37_1742-32dup
NM_001278138.1:c.1196-37_1196-32dup	NP_001265067.1:n.1196-37_1196-32dup
XM_011519273.1:c.-493_-488dup	XP_011517575.1:n.-493_-488dup
NR_136302.1:n.21_26dup
NM_001114753.3:c.1742-37_1742-32dup MANE Select	NP_001108225.1:n.1742-37_1742-32dup
NM_001278138.2:c.1196-37_1196-32dup	NP_001265067.1:n.1196-37_1196-32dup