Canonical Allele Identifier: CA2691806446

Gene: ENG

Linked Data

• gnomAD v4: 9-127819462-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127819462A>C , CM000671.2:g.127819462A>C	GRCh38
NC_000009.11:g.130581741A>C , CM000671.1:g.130581741A>C	GRCh37
NC_000009.10:g.129621562A>C	NCBI36
NG_009551.1:g.40307T>G , LRG_589:g.40307T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000480266.6:c.765+160T>G	ENSP00000479015.1:n.765+160T>G
ENST00000373203.9:c.1311+160T>G MANE Select	ENSP00000362299.4:n.1311+160T>G
ENST00000344849.4:c.1311+160T>G	ENSP00000341917.3:n.1311+160T>G
ENST00000373203.8:c.1311+160T>G	ENSP00000362299.4:n.1311+160T>G
ENST00000480266.5:c.765+160T>G	ENSP00000479015.1:n.765+160T>G
ENST00000486329.1:n.439T>G
NM_000118.3:c.1311+160T>G , LRG_589t1:c.1311+160T>G	NP_000109.1:n.1311+160T>G
NM_001114753.2:c.1311+160T>G , LRG_589t2:c.1311+160T>G	NP_001108225.1:n.1311+160T>G
NM_001278138.1:c.765+160T>G	NP_001265067.1:n.765+160T>G
NR_136302.1:n.1568+751A>C
NM_001114753.3:c.1311+160T>G MANE Select	NP_001108225.1:n.1311+160T>G
NM_001278138.2:c.765+160T>G	NP_001265067.1:n.765+160T>G