Canonical Allele Identifier: CA2627629492

Gene: EMC4

Linked Data

• gnomAD v4: 15-34228307-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34228307C>A , CM000677.2:g.34228307C>A	GRCh38
NC_000015.9:g.34520508C>A , CM000677.1:g.34520508C>A	GRCh37
NC_000015.8:g.32307800C>A	NCBI36
NG_007951.1:g.114758G>T , LRG_270:g.114758G>T
NG_054746.1:g.8311C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000267750.9:c.356-122C>A MANE Select	ENSP00000267750.4:n.356-122C>A
ENST00000249209.8:c.355+461C>A	ENSP00000249209.4:n.355+461C>A
ENST00000267750.8:c.356-122C>A	ENSP00000267750.4:n.356-122C>A
ENST00000557879.1:c.*179C>A	ENSP00000473881.1:n.*179C>A
ENST00000558102.1:c.*108+461C>A	ENSP00000453880.1:n.*108+461C>A
ENST00000558205.5:c.*109-122C>A	ENSP00000454042.1:n.*109-122C>A
ENST00000559078.5:c.303+513C>A	ENSP00000454052.1:n.303+513C>A
ENST00000559421.1:c.202-1446C>A	ENSP00000452672.1:n.202-1446C>A
ENST00000560911.5:c.*109-122C>A	ENSP00000453610.1:n.*109-122C>A
ENST00000560947.1:c.153-130C>A
ENST00000561246.1:n.1313+483C>A
NM_001286420.1:c.355+461C>A	NP_001273349.1:n.355+461C>A
NM_016454.3:c.356-122C>A	NP_057538.1:n.356-122C>A
NM_001351373.1:c.113-122C>A	NP_001338302.1:n.113-122C>A
NR_147140.1:n.481+461C>A
NM_016454.4:c.356-122C>A MANE Select	NP_057538.1:n.356-122C>A
NM_001286420.2:c.355+461C>A	NP_001273349.1:n.355+461C>A
NM_001351373.2:c.113-122C>A	NP_001338302.1:n.113-122C>A
NR_147140.2:n.462+461C>A