Canonical Allele Identifier: CA1879982041

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127829822_127829823delinsCG , CM000671.2:g.127829822_127829823delinsCG	GRCh38
NC_000009.11:g.130592101_130592102delinsCG , CM000671.1:g.130592101_130592102delinsCG	GRCh37
NC_000009.10:g.129631922_129631923delinsCG	NCBI36
NG_009551.1:g.29946_29947delinsCG , LRG_589:g.29946_29947delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.-323_-322delinsCG	ENSP00000479015.1:n.-323_-322delinsCG
ENST00000373203.9:c.224_225delinsCG MANE Select	ENSP00000362299.4:p.Pro75=
ENST00000344849.4:c.224_225delinsCG	ENSP00000341917.3:p.Pro75=
ENST00000373203.8:c.224_225delinsCG	ENSP00000362299.4:p.Pro75=
ENST00000480266.5:c.-323_-322delinsCG	ENSP00000479015.1:n.-323_-322delinsCG
NM_000118.3:c.224_225delinsCG , LRG_589t1:c.224_225delinsCG	NP_000109.1:p.Pro75=
NM_001114753.2:c.224_225delinsCG , LRG_589t2:c.224_225delinsCG	NP_001108225.1:p.Pro75=
NM_001278138.1:c.-323_-322delinsCG	NP_001265067.1:n.-323_-322delinsCG
XR_001746952.2:n.83-2576_83-2575delinsCG
NM_001114753.3:c.224_225delinsCG MANE Select	NP_001108225.1:p.Pro75=
NM_001278138.2:c.-323_-322delinsCG	NP_001265067.1:n.-323_-322delinsCG