Canonical Allele Identifier: CA467232192

Gene: ENG

Linked Data

• MyVariant Identifiers: chr9:g.130592005C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127829726C>G , CM000671.2:g.127829726C>G	GRCh38
NC_000009.11:g.130592005C>G , CM000671.1:g.130592005C>G	GRCh37
NC_000009.10:g.129631826C>G	NCBI36
NG_009551.1:g.30043G>C , LRG_589:g.30043G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.-226G>C	ENSP00000479015.1:n.-226G>C
ENST00000373203.9:c.321G>C MANE Select	ENSP00000362299.4:p.Leu107=
ENST00000344849.4:c.321G>C	ENSP00000341917.3:p.Leu107=
ENST00000373203.8:c.321G>C	ENSP00000362299.4:p.Leu107=
ENST00000462196.1:n.79G>C
ENST00000480266.5:c.-226G>C	ENSP00000479015.1:n.-226G>C
NM_000118.3:c.321G>C , LRG_589t1:c.321G>C	NP_000109.1:p.Leu107=
NM_001114753.2:c.321G>C , LRG_589t2:c.321G>C	NP_001108225.1:p.Leu107=
NM_001278138.1:c.-226G>C	NP_001265067.1:n.-226G>C
XR_001746952.2:n.83-2672C>G
NM_001114753.3:c.321G>C MANE Select	NP_001108225.1:p.Leu107=
NM_001278138.2:c.-226G>C	NP_001265067.1:n.-226G>C