Canonical Allele Identifier: CA2785996380

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127815141T>G , CM000671.2:g.127815141T>G	GRCh38
NC_000009.11:g.130577420T>G , CM000671.1:g.130577420T>G	GRCh37
NC_000009.10:g.129617241T>G	NCBI36
NG_009551.1:g.44628A>C , LRG_589:g.44628A>C
NG_023245.1:g.17267T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.*541A>C	ENSP00000479015.1:n.*541A>C
ENST00000373203.9:c.*541A>C MANE Select	ENSP00000362299.4:n.*541A>C
ENST00000344849.4:c.*776A>C	ENSP00000341917.3:n.*776A>C
ENST00000373203.8:c.*541A>C	ENSP00000362299.4:n.*541A>C
ENST00000480266.5:c.*541A>C	ENSP00000479015.1:n.*541A>C
NM_000118.3:c.*776A>C , LRG_589t1:c.*776A>C	NP_000109.1:n.*776A>C
NM_001114753.2:c.*541A>C , LRG_589t2:c.*541A>C	NP_001108225.1:n.*541A>C
NM_001278138.1:c.*541A>C	NP_001265067.1:n.*541A>C
NM_001114753.3:c.*541A>C MANE Select	NP_001108225.1:n.*541A>C
NM_001278138.2:c.*541A>C	NP_001265067.1:n.*541A>C