Canonical Allele Identifier: CA2466663628

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379317_154379318delinsGA , CM000685.2:g.154379317_154379318delinsGA	GRCh38
NC_000023.10:g.153607677_153607678delinsGA , CM000685.1:g.153607677_153607678delinsGA	GRCh37
NC_000023.9:g.153260871_153260872delinsGA	NCBI36
NG_008677.1:g.9882_9883delinsGA , LRG_745:g.9882_9883delinsGA
NG_011506.1:g.329_330delinsTC
NG_011506.2:g.321_322delinsTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000369842.9:c.-168_-167delinsGA MANE Select	ENSP00000358857.4:n.-168_-167delinsGA
ENST00000369835.3:c.-168_-167delinsGA	ENSP00000358850.3:n.-168_-167delinsGA
ENST00000369842.8:c.-168_-167delinsGA	ENSP00000358857.4:n.-168_-167delinsGA
NM_000117.2:c.-168_-167delinsGA , LRG_745t1:c.-168_-167delinsGA	NP_000108.1:n.-168_-167delinsGA
XM_024452349.1:c.-376_-375delinsGA	XP_024308117.1:n.-376_-375delinsGA
NM_000117.3:c.-168_-167delinsGA MANE Select	NP_000108.1:n.-168_-167delinsGA