Canonical Allele Identifier: CA374989588

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127854315A>G , CM000671.2:g.127854315A>G	GRCh38
NC_000009.11:g.130616594A>G , CM000671.1:g.130616594A>G	GRCh37
NC_000009.10:g.129656415A>G	NCBI36
NG_009551.1:g.5454T>C , LRG_589:g.5454T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001114753.3:c.41T>C MANE Select	NP_001108225.1:p.Leu14Pro
ENST00000373203.9:c.41T>C MANE Select	ENSP00000362299.4:p.Leu14Pro
NM_000118.3:c.41T>C , LRG_589t1:c.41T>C	NP_000109.1:p.Leu14Pro
NM_001114753.2:c.41T>C , LRG_589t2:c.41T>C	NP_001108225.1:p.Leu14Pro
ENST00000344849.4:c.41T>C	ENSP00000341917.3:p.Leu14Pro
ENST00000373203.8:c.41T>C	ENSP00000362299.4:p.Leu14Pro