Canonical Allele Identifier: CA374971515

Gene: ENG

Linked Data

• ClinVar Variation Id: 2999407
• ClinVar RCV Id: RCV003852038
• gnomAD v4: 9-127815943-G-C
• MyVariant Identifiers: chr9:g.130578222G>C (hg19) ; chr9:g.127815943G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127815943G>C , CM000671.2:g.127815943G>C	GRCh38
NC_000009.11:g.130578222G>C , CM000671.1:g.130578222G>C	GRCh37
NC_000009.10:g.129618043G>C	NCBI36
NG_009551.1:g.43826C>G , LRG_589:g.43826C>G
NG_023245.1:g.18069G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.1306C>G	ENSP00000479015.1:p.Arg436Gly
ENST00000373203.9:c.1852C>G MANE Select	ENSP00000362299.4:p.Arg618Gly
ENST00000344849.4:c.1852C>G	ENSP00000341917.3:p.Arg618Gly
ENST00000373203.8:c.1852C>G	ENSP00000362299.4:p.Arg618Gly
ENST00000480266.5:c.1306C>G	ENSP00000479015.1:p.Arg436Gly
NM_000118.3:c.1852C>G , LRG_589t1:c.1852C>G	NP_000109.1:p.Arg618Gly
NM_001114753.2:c.1852C>G , LRG_589t2:c.1852C>G	NP_001108225.1:p.Arg618Gly
NM_001278138.1:c.1306C>G	NP_001265067.1:p.Arg436Gly
NM_001114753.3:c.1852C>G MANE Select	NP_001108225.1:p.Arg618Gly
NM_001278138.2:c.1306C>G	NP_001265067.1:p.Arg436Gly