Canonical Allele Identifier: CA2627629597

Gene: EMC4

Linked Data

• gnomAD v4: 15-34228396-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34228400del , CM000677.2:g.34228400del	GRCh38
NC_000015.9:g.34520601del , CM000677.1:g.34520601del	GRCh37
NC_000015.8:g.32307893del	NCBI36
NG_007951.1:g.114668del , LRG_270:g.114668del
NG_054746.1:g.8404del

Transcript Alleles

HGVS	Amino-acid change
ENST00000267750.9:c.356-29del MANE Select	ENSP00000267750.4:n.356-29del
ENST00000249209.8:c.355+554del	ENSP00000249209.4:n.355+554del
ENST00000267750.8:c.356-29del	ENSP00000267750.4:n.356-29del
ENST00000557879.1:c.*272del	ENSP00000473881.1:n.*272del
ENST00000558102.1:c.*108+554del	ENSP00000453880.1:n.*108+554del
ENST00000558205.5:c.*109-29del	ENSP00000454042.1:n.*109-29del
ENST00000559078.5:c.304-566del	ENSP00000454052.1:n.304-566del
ENST00000559421.1:c.202-1353del	ENSP00000452672.1:n.202-1353del
ENST00000560911.5:c.*109-29del	ENSP00000453610.1:n.*109-29del
ENST00000560947.1:c.153-37del
ENST00000561246.1:n.1313+576del
NM_001286420.1:c.355+554del	NP_001273349.1:n.355+554del
NM_016454.3:c.356-29del	NP_057538.1:n.356-29del
NM_001351373.1:c.113-29del	NP_001338302.1:n.113-29del
NR_147140.1:n.481+554del
NM_016454.4:c.356-29del MANE Select	NP_057538.1:n.356-29del
NM_001286420.2:c.355+554del	NP_001273349.1:n.355+554del
NM_001351373.2:c.113-29del	NP_001338302.1:n.113-29del
NR_147140.2:n.462+554del