Canonical Allele Identifier: CA1879982132

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127816124_127816125delinsCA , CM000671.2:g.127816124_127816125delinsCA	GRCh38
NC_000009.11:g.130578403_130578404delinsCA , CM000671.1:g.130578403_130578404delinsCA	GRCh37
NC_000009.10:g.129618224_129618225delinsCA	NCBI36
NG_009551.1:g.43644_43645delinsTG , LRG_589:g.43644_43645delinsTG
NG_023245.1:g.18250_18251delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.1196-72_1196-71delinsTG	ENSP00000479015.1:n.1196-72_1196-71delinsTG
ENST00000373203.9:c.1742-72_1742-71delinsTG MANE Select	ENSP00000362299.4:n.1742-72_1742-71delinsTG
ENST00000344849.4:c.1742-72_1742-71delinsTG	ENSP00000341917.3:n.1742-72_1742-71delinsTG
ENST00000373203.8:c.1742-72_1742-71delinsTG	ENSP00000362299.4:n.1742-72_1742-71delinsTG
ENST00000480266.5:c.1196-72_1196-71delinsTG	ENSP00000479015.1:n.1196-72_1196-71delinsTG
NM_000118.3:c.1742-72_1742-71delinsTG , LRG_589t1:c.1742-72_1742-71delinsTG	NP_000109.1:n.1742-72_1742-71delinsTG
NM_001114753.2:c.1742-72_1742-71delinsTG , LRG_589t2:c.1742-72_1742-71delinsTG	NP_001108225.1:n.1742-72_1742-71delinsTG
NM_001278138.1:c.1196-72_1196-71delinsTG	NP_001265067.1:n.1196-72_1196-71delinsTG
XM_011519273.1:c.-455_-454delinsCA	XP_011517575.1:n.-455_-454delinsCA
NR_136302.1:n.59_60delinsCA
NM_001114753.3:c.1742-72_1742-71delinsTG MANE Select	NP_001108225.1:n.1742-72_1742-71delinsTG
NM_001278138.2:c.1196-72_1196-71delinsTG	NP_001265067.1:n.1196-72_1196-71delinsTG