Canonical Allele Identifier: CA200319804

Gene: ENG

Linked Data

• dbSNP Id: rs902714680
• MyVariant Identifiers: chr9:g.130602439G>C (hg19) ; chr9:g.127840160G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127840160G>C , CM000671.2:g.127840160G>C	GRCh38
NC_000009.11:g.130602439G>C , CM000671.1:g.130602439G>C	GRCh37
NC_000009.10:g.129642260G>C	NCBI36
NG_009551.1:g.19609C>G , LRG_589:g.19609C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000480266.6:c.-328+2934C>G	ENSP00000479015.1:n.-328+2934C>G
ENST00000373203.9:c.219+2934C>G MANE Select	ENSP00000362299.4:n.219+2934C>G
ENST00000344849.4:c.219+2934C>G	ENSP00000341917.3:n.219+2934C>G
ENST00000373203.8:c.219+2934C>G	ENSP00000362299.4:n.219+2934C>G
ENST00000480266.5:c.-328+2934C>G	ENSP00000479015.1:n.-328+2934C>G
NM_000118.3:c.219+2934C>G , LRG_589t1:c.219+2934C>G	NP_000109.1:n.219+2934C>G
NM_001114753.2:c.219+2934C>G , LRG_589t2:c.219+2934C>G	NP_001108225.1:n.219+2934C>G
NM_001278138.1:c.-328+2934C>G	NP_001265067.1:n.-328+2934C>G
NM_001114753.3:c.219+2934C>G MANE Select	NP_001108225.1:n.219+2934C>G
NM_001278138.2:c.-328+2934C>G	NP_001265067.1:n.-328+2934C>G