Canonical Allele Identifier: CA1879990595

Gene: ENG

Linked Data

• dbSNP Id: rs1588577376

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127820411T>G , CM000671.2:g.127820411T>G	GRCh38
NC_000009.11:g.130582690T>G , CM000671.1:g.130582690T>G	GRCh37
NC_000009.10:g.129622511T>G	NCBI36
NG_009551.1:g.39358A>C , LRG_589:g.39358A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.589-374A>C	ENSP00000479015.1:n.589-374A>C
ENST00000373203.9:c.1135-374A>C MANE Select	ENSP00000362299.4:n.1135-374A>C
ENST00000344849.4:c.1135-374A>C	ENSP00000341917.3:n.1135-374A>C
ENST00000373203.8:c.1135-374A>C	ENSP00000362299.4:n.1135-374A>C
ENST00000480266.5:c.589-374A>C	ENSP00000479015.1:n.589-374A>C
ENST00000486329.1:n.103-374A>C
NM_000118.3:c.1135-374A>C , LRG_589t1:c.1135-374A>C	NP_000109.1:n.1135-374A>C
NM_001114753.2:c.1135-374A>C , LRG_589t2:c.1135-374A>C	NP_001108225.1:n.1135-374A>C
NM_001278138.1:c.589-374A>C	NP_001265067.1:n.589-374A>C
NR_136302.1:n.1569-784T>G
NM_001114753.3:c.1135-374A>C MANE Select	NP_001108225.1:n.1135-374A>C
NM_001278138.2:c.589-374A>C	NP_001265067.1:n.589-374A>C