Canonical Allele Identifier: CA391615904

Gene: EMC4

Linked Data

• MyVariant Identifiers: chr15:g.34520633T>C (hg19) ; chr15:g.34228432T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34228432T>C , CM000677.2:g.34228432T>C	GRCh38
NC_000015.9:g.34520633T>C , CM000677.1:g.34520633T>C	GRCh37
NC_000015.8:g.32307925T>C	NCBI36
NG_007951.1:g.114633A>G , LRG_270:g.114633A>G
NG_054746.1:g.8436T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000267750.9:c.359T>C MANE Select	ENSP00000267750.4:p.Phe120Ser
ENST00000249209.8:c.355+586T>C	ENSP00000249209.4:n.355+586T>C
ENST00000267750.8:c.359T>C	ENSP00000267750.4:p.Phe120Ser
ENST00000557879.1:c.*304T>C	ENSP00000473881.1:n.*304T>C
ENST00000558102.1:c.*108+586T>C	ENSP00000453880.1:n.*108+586T>C
ENST00000558205.5:c.*112T>C	ENSP00000454042.1:n.*112T>C
ENST00000559078.5:c.304-534T>C	ENSP00000454052.1:n.304-534T>C
ENST00000559421.1:c.202-1321T>C	ENSP00000452672.1:n.202-1321T>C
ENST00000560911.5:c.*112T>C	ENSP00000453610.1:n.*112T>C
ENST00000560947.1:c.153-5T>C
ENST00000561246.1:n.1313+608T>C
NM_001286420.1:c.355+586T>C	NP_001273349.1:n.355+586T>C
NM_016454.3:c.359T>C	NP_057538.1:p.Phe120Ser
NM_001351373.1:c.116T>C	NP_001338302.1:p.Phe39Ser
NR_147140.1:n.481+586T>C
NM_016454.4:c.359T>C MANE Select	NP_057538.1:p.Phe120Ser
NM_001286420.2:c.355+586T>C	NP_001273349.1:n.355+586T>C
NM_001351373.2:c.116T>C	NP_001338302.1:p.Phe39Ser
NR_147140.2:n.462+586T>C