Canonical Allele Identifier: CA374984149

Gene: ENG

Linked Data

• ClinVar Variation Id: 854634
• ClinVar RCV Id: RCV001059724
• dbSNP Id: rs1830620321
• MyVariant Identifiers: chr9:g.130588818G>A (hg19) ; chr9:g.127826539G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127826539G>A , CM000671.2:g.127826539G>A	GRCh38
NC_000009.11:g.130588818G>A , CM000671.1:g.130588818G>A	GRCh37
NC_000009.10:g.129628639G>A	NCBI36
NG_009551.1:g.33230C>T , LRG_589:g.33230C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000480266.6:c.-53C>T	ENSP00000479015.1:n.-53C>T
ENST00000373203.9:c.494C>T MANE Select	ENSP00000362299.4:p.Pro165Leu
ENST00000344849.4:c.494C>T	ENSP00000341917.3:p.Pro165Leu
ENST00000373203.8:c.494C>T	ENSP00000362299.4:p.Pro165Leu
ENST00000462196.1:n.394C>T
ENST00000480266.5:c.-53C>T	ENSP00000479015.1:n.-53C>T
NM_000118.3:c.494C>T , LRG_589t1:c.494C>T	NP_000109.1:p.Pro165Leu
NM_001114753.2:c.494C>T , LRG_589t2:c.494C>T	NP_001108225.1:p.Pro165Leu
NM_001278138.1:c.-53C>T	NP_001265067.1:n.-53C>T
XR_001746952.2:n.82+1081G>A
NM_001114753.3:c.494C>T MANE Select	NP_001108225.1:p.Pro165Leu
NM_001278138.2:c.-53C>T	NP_001265067.1:n.-53C>T