Canonical Allele Identifier: CA374974237
Gene: ENG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127818175G>T , CM000671.2:g.127818175G>T GRCh38
NC_000009.11:g.130580454G>T , CM000671.1:g.130580454G>T GRCh37
NC_000009.10:g.129620275G>T NCBI36
NG_009551.1:g.41594C>A , LRG_589:g.41594C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000480266.6:c.1085C>A ENSP00000479015.1:p.Thr362Asn
ENST00000373203.9:c.1631C>A MANE Select ENSP00000362299.4:p.Thr544Asn
ENST00000344849.4:c.1631C>A ENSP00000341917.3:p.Thr544Asn
ENST00000373203.8:c.1631C>A ENSP00000362299.4:p.Thr544Asn
ENST00000480266.5:c.1085C>A ENSP00000479015.1:p.Thr362Asn
NM_000118.3:c.1631C>A , LRG_589t1:c.1631C>A NP_000109.1:p.Thr544Asn
NM_001114753.2:c.1631C>A , LRG_589t2:c.1631C>A NP_001108225.1:p.Thr544Asn
NM_001278138.1:c.1085C>A NP_001265067.1:p.Thr362Asn
NR_136302.1:n.1378-136G>T
NM_001114753.3:c.1631C>A MANE Select NP_001108225.1:p.Thr544Asn
NM_001278138.2:c.1085C>A NP_001265067.1:p.Thr362Asn