Canonical Allele Identifier: CA374972114
Gene: ENG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127816008G>C , CM000671.2:g.127816008G>C GRCh38
NC_000009.11:g.130578287G>C , CM000671.1:g.130578287G>C GRCh37
NC_000009.10:g.129618108G>C NCBI36
NG_009551.1:g.43761C>G , LRG_589:g.43761C>G
NG_023245.1:g.18134G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000480266.6:c.1241C>G ENSP00000479015.1:p.Thr414Ser
ENST00000373203.9:c.1787C>G MANE Select ENSP00000362299.4:p.Thr596Ser
ENST00000344849.4:c.1787C>G ENSP00000341917.3:p.Thr596Ser
ENST00000373203.8:c.1787C>G ENSP00000362299.4:p.Thr596Ser
ENST00000480266.5:c.1241C>G ENSP00000479015.1:p.Thr414Ser
NM_000118.3:c.1787C>G , LRG_589t1:c.1787C>G NP_000109.1:p.Thr596Ser
NM_001114753.2:c.1787C>G , LRG_589t2:c.1787C>G NP_001108225.1:p.Thr596Ser
NM_001278138.1:c.1241C>G NP_001265067.1:p.Thr414Ser
NM_001114753.3:c.1787C>G MANE Select NP_001108225.1:p.Thr596Ser
NM_001278138.2:c.1241C>G NP_001265067.1:p.Thr414Ser