Canonical Allele Identifier: CA2691806667

Gene: ENG

Linked Data

• gnomAD v4: 9-127820091-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127820091_127820092insT , CM000671.2:g.127820091_127820092insT	GRCh38
NC_000009.11:g.130582370_130582371insT , CM000671.1:g.130582370_130582371insT	GRCh37
NC_000009.10:g.129622191_129622192insT	NCBI36
NG_009551.1:g.39677_39678insA , LRG_589:g.39677_39678insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.589-55_589-54insA	ENSP00000479015.1:n.589-55_589-54insA
ENST00000373203.9:c.1135-55_1135-54insA MANE Select	ENSP00000362299.4:n.1135-55_1135-54insA
ENST00000344849.4:c.1135-55_1135-54insA	ENSP00000341917.3:n.1135-55_1135-54insA
ENST00000373203.8:c.1135-55_1135-54insA	ENSP00000362299.4:n.1135-55_1135-54insA
ENST00000480266.5:c.589-55_589-54insA	ENSP00000479015.1:n.589-55_589-54insA
ENST00000486329.1:n.103-55_103-54insA
NM_000118.3:c.1135-55_1135-54insA , LRG_589t1:c.1135-55_1135-54insA	NP_000109.1:n.1135-55_1135-54insA
NM_001114753.2:c.1135-55_1135-54insA , LRG_589t2:c.1135-55_1135-54insA	NP_001108225.1:n.1135-55_1135-54insA
NM_001278138.1:c.589-55_589-54insA	NP_001265067.1:n.589-55_589-54insA
NR_136302.1:n.1569-1104_1569-1103insT
NM_001114753.3:c.1135-55_1135-54insA MANE Select	NP_001108225.1:n.1135-55_1135-54insA
NM_001278138.2:c.589-55_589-54insA	NP_001265067.1:n.589-55_589-54insA