Canonical Allele Identifier: CA2627629482

Gene: EMC4

Linked Data

• gnomAD v4: 15-34228300-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34228300T>C , CM000677.2:g.34228300T>C	GRCh38
NC_000015.9:g.34520501T>C , CM000677.1:g.34520501T>C	GRCh37
NC_000015.8:g.32307793T>C	NCBI36
NG_007951.1:g.114765A>G , LRG_270:g.114765A>G
NG_054746.1:g.8304T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267750.9:c.356-129T>C MANE Select	ENSP00000267750.4:n.356-129T>C
ENST00000249209.8:c.355+454T>C	ENSP00000249209.4:n.355+454T>C
ENST00000267750.8:c.356-129T>C	ENSP00000267750.4:n.356-129T>C
ENST00000557879.1:c.*172T>C	ENSP00000473881.1:n.*172T>C
ENST00000558102.1:c.*108+454T>C	ENSP00000453880.1:n.*108+454T>C
ENST00000558205.5:c.*109-129T>C	ENSP00000454042.1:n.*109-129T>C
ENST00000559078.5:c.303+506T>C	ENSP00000454052.1:n.303+506T>C
ENST00000559421.1:c.202-1453T>C	ENSP00000452672.1:n.202-1453T>C
ENST00000560911.5:c.*109-129T>C	ENSP00000453610.1:n.*109-129T>C
ENST00000560947.1:c.153-137T>C
ENST00000561246.1:n.1313+476T>C
NM_001286420.1:c.355+454T>C	NP_001273349.1:n.355+454T>C
NM_016454.3:c.356-129T>C	NP_057538.1:n.356-129T>C
NM_001351373.1:c.113-129T>C	NP_001338302.1:n.113-129T>C
NR_147140.1:n.481+454T>C
NM_016454.4:c.356-129T>C MANE Select	NP_057538.1:n.356-129T>C
NM_001286420.2:c.355+454T>C	NP_001273349.1:n.355+454T>C
NM_001351373.2:c.113-129T>C	NP_001338302.1:n.113-129T>C
NR_147140.2:n.462+454T>C