Canonical Allele Identifier: CA7463718

Gene: EMC4

Linked Data

• dbSNP Id: rs775374398
• ExAC: 15:34520643 A / G
• gnomAD v2: 15-34520643-A-G
• gnomAD v4: 15-34228442-A-G
• MyVariant Identifiers: chr15:g.34520643A>G (hg19) ; chr15:g.34228442A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34228442A>G , CM000677.2:g.34228442A>G	GRCh38
NC_000015.9:g.34520643A>G , CM000677.1:g.34520643A>G	GRCh37
NC_000015.8:g.32307935A>G	NCBI36
NG_007951.1:g.114623T>C , LRG_270:g.114623T>C
NG_054746.1:g.8446A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267750.9:c.369A>G MANE Select	ENSP00000267750.4:p.Leu123=
ENST00000249209.8:c.355+596A>G	ENSP00000249209.4:n.355+596A>G
ENST00000267750.8:c.369A>G	ENSP00000267750.4:p.Leu123=
ENST00000557879.1:c.*314A>G	ENSP00000473881.1:n.*314A>G
ENST00000558102.1:c.*108+596A>G	ENSP00000453880.1:n.*108+596A>G
ENST00000558205.5:c.*122A>G	ENSP00000454042.1:n.*122A>G
ENST00000559078.5:c.304-524A>G	ENSP00000454052.1:n.304-524A>G
ENST00000559421.1:c.202-1311A>G	ENSP00000452672.1:n.202-1311A>G
ENST00000560911.5:c.*122A>G	ENSP00000453610.1:n.*122A>G
ENST00000560947.1:c.158A>G
ENST00000561246.1:n.1313+618A>G
NM_001286420.1:c.355+596A>G	NP_001273349.1:n.355+596A>G
NM_016454.3:c.369A>G	NP_057538.1:p.Leu123=
NM_001351373.1:c.126A>G	NP_001338302.1:p.Leu42=
NR_147140.1:n.481+596A>G
NM_016454.4:c.369A>G MANE Select	NP_057538.1:p.Leu123=
NM_001286420.2:c.355+596A>G	NP_001273349.1:n.355+596A>G
NM_001351373.2:c.126A>G	NP_001338302.1:p.Leu42=
NR_147140.2:n.462+596A>G