Canonical Allele Identifier: CA391616037

Gene: EMC4

Linked Data

• MyVariant Identifiers: chr15:g.34520690G>C (hg19) ; chr15:g.34228489G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34228489G>C , CM000677.2:g.34228489G>C	GRCh38
NC_000015.9:g.34520690G>C , CM000677.1:g.34520690G>C	GRCh37
NC_000015.8:g.32307982G>C	NCBI36
NG_007951.1:g.114576C>G , LRG_270:g.114576C>G
NG_054746.1:g.8493G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000267750.9:c.416G>C MANE Select	ENSP00000267750.4:p.Gly139Ala
ENST00000249209.8:c.355+643G>C	ENSP00000249209.4:n.355+643G>C
ENST00000267750.8:c.416G>C	ENSP00000267750.4:p.Gly139Ala
ENST00000557879.1:c.*361G>C	ENSP00000473881.1:n.*361G>C
ENST00000558102.1:c.*108+643G>C	ENSP00000453880.1:n.*108+643G>C
ENST00000558205.5:c.*169G>C	ENSP00000454042.1:n.*169G>C
ENST00000559078.5:c.304-477G>C	ENSP00000454052.1:n.304-477G>C
ENST00000559421.1:c.202-1264G>C	ENSP00000452672.1:n.202-1264G>C
ENST00000560911.5:c.*169G>C	ENSP00000453610.1:n.*169G>C
ENST00000560947.1:c.205G>C
ENST00000561246.1:n.1313+665G>C
NM_001286420.1:c.355+643G>C	NP_001273349.1:n.355+643G>C
NM_016454.3:c.416G>C	NP_057538.1:p.Gly139Ala
NM_001351373.1:c.173G>C	NP_001338302.1:p.Gly58Ala
NR_147140.1:n.481+643G>C
NM_016454.4:c.416G>C MANE Select	NP_057538.1:p.Gly139Ala
NM_001286420.2:c.355+643G>C	NP_001273349.1:n.355+643G>C
NM_001351373.2:c.173G>C	NP_001338302.1:p.Gly58Ala
NR_147140.2:n.462+643G>C