Canonical Allele Identifier: CA391616032

Gene: EMC4

Linked Data

• MyVariant Identifiers: chr15:g.34520688T>G (hg19) ; chr15:g.34228487T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34228487T>G , CM000677.2:g.34228487T>G	GRCh38
NC_000015.9:g.34520688T>G , CM000677.1:g.34520688T>G	GRCh37
NC_000015.8:g.32307980T>G	NCBI36
NG_007951.1:g.114578A>C , LRG_270:g.114578A>C
NG_054746.1:g.8491T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000267750.9:c.414T>G MANE Select	ENSP00000267750.4:p.Ile138Met
ENST00000249209.8:c.355+641T>G	ENSP00000249209.4:n.355+641T>G
ENST00000267750.8:c.414T>G	ENSP00000267750.4:p.Ile138Met
ENST00000557879.1:c.*359T>G	ENSP00000473881.1:n.*359T>G
ENST00000558102.1:c.*108+641T>G	ENSP00000453880.1:n.*108+641T>G
ENST00000558205.5:c.*167T>G	ENSP00000454042.1:n.*167T>G
ENST00000559078.5:c.304-479T>G	ENSP00000454052.1:n.304-479T>G
ENST00000559421.1:c.202-1266T>G	ENSP00000452672.1:n.202-1266T>G
ENST00000560911.5:c.*167T>G	ENSP00000453610.1:n.*167T>G
ENST00000560947.1:c.203T>G
ENST00000561246.1:n.1313+663T>G
NM_001286420.1:c.355+641T>G	NP_001273349.1:n.355+641T>G
NM_016454.3:c.414T>G	NP_057538.1:p.Ile138Met
NM_001351373.1:c.171T>G	NP_001338302.1:p.Ile57Met
NR_147140.1:n.481+641T>G
NM_016454.4:c.414T>G MANE Select	NP_057538.1:p.Ile138Met
NM_001286420.2:c.355+641T>G	NP_001273349.1:n.355+641T>G
NM_001351373.2:c.171T>G	NP_001338302.1:p.Ile57Met
NR_147140.2:n.462+641T>G