Canonical Allele Identifier: CA2691810562
Gene: ENG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127854270T>C , CM000671.2:g.127854270T>C GRCh38
NC_000009.11:g.130616549T>C , CM000671.1:g.130616549T>C GRCh37
NC_000009.10:g.129656370T>C NCBI36
NG_009551.1:g.5499A>G , LRG_589:g.5499A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000373203.9:c.67+19A>G MANE Select ENSP00000362299.4:n.67+19A>G
ENST00000344849.4:c.67+19A>G ENSP00000341917.3:n.67+19A>G
ENST00000373203.8:c.67+19A>G ENSP00000362299.4:n.67+19A>G
NM_000118.3:c.67+19A>G , LRG_589t1:c.67+19A>G NP_000109.1:n.67+19A>G
NM_001114753.2:c.67+19A>G , LRG_589t2:c.67+19A>G NP_001108225.1:n.67+19A>G
NM_001114753.3:c.67+19A>G MANE Select NP_001108225.1:n.67+19A>G