Canonical Allele Identifier: CA374972274
Gene: ENG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127816035A>G , CM000671.2:g.127816035A>G GRCh38
NC_000009.11:g.130578314A>G , CM000671.1:g.130578314A>G GRCh37
NC_000009.10:g.129618135A>G NCBI36
NG_009551.1:g.43734T>C , LRG_589:g.43734T>C
NG_023245.1:g.18161A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000480266.6:c.1214T>C ENSP00000479015.1:p.Leu405Pro
ENST00000373203.9:c.1760T>C MANE Select ENSP00000362299.4:p.Leu587Pro
ENST00000344849.4:c.1760T>C ENSP00000341917.3:p.Leu587Pro
ENST00000373203.8:c.1760T>C ENSP00000362299.4:p.Leu587Pro
ENST00000480266.5:c.1214T>C ENSP00000479015.1:p.Leu405Pro
NM_000118.3:c.1760T>C , LRG_589t1:c.1760T>C NP_000109.1:p.Leu587Pro
NM_001114753.2:c.1760T>C , LRG_589t2:c.1760T>C NP_001108225.1:p.Leu587Pro
NM_001278138.1:c.1214T>C NP_001265067.1:p.Leu405Pro
NM_001114753.3:c.1760T>C MANE Select NP_001108225.1:p.Leu587Pro
NM_001278138.2:c.1214T>C NP_001265067.1:p.Leu405Pro