Canonical Allele Identifier: CA2691806689
Gene: ENG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127820113_127820122dup , CM000671.2:g.127820113_127820122dup GRCh38
NC_000009.11:g.130582392_130582401dup , CM000671.1:g.130582392_130582401dup GRCh37
NC_000009.10:g.129622213_129622222dup NCBI36
NG_009551.1:g.39647_39656dup , LRG_589:g.39647_39656dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000480266.6:c.589-85_589-76dup ENSP00000479015.1:n.589-85_589-76dup
ENST00000373203.9:c.1135-85_1135-76dup MANE Select ENSP00000362299.4:n.1135-85_1135-76dup
ENST00000344849.4:c.1135-85_1135-76dup ENSP00000341917.3:n.1135-85_1135-76dup
ENST00000373203.8:c.1135-85_1135-76dup ENSP00000362299.4:n.1135-85_1135-76dup
ENST00000480266.5:c.589-85_589-76dup ENSP00000479015.1:n.589-85_589-76dup
ENST00000486329.1:n.103-85_103-76dup
NM_000118.3:c.1135-85_1135-76dup , LRG_589t1:c.1135-85_1135-76dup NP_000109.1:n.1135-85_1135-76dup
NM_001114753.2:c.1135-85_1135-76dup , LRG_589t2:c.1135-85_1135-76dup NP_001108225.1:n.1135-85_1135-76dup
NM_001278138.1:c.589-85_589-76dup NP_001265067.1:n.589-85_589-76dup
NR_136302.1:n.1569-1082_1569-1073dup
NM_001114753.3:c.1135-85_1135-76dup MANE Select NP_001108225.1:n.1135-85_1135-76dup
NM_001278138.2:c.589-85_589-76dup NP_001265067.1:n.589-85_589-76dup