Canonical Allele Identifier: CA2466664274

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380726_154380742delinsTCCCCTCGCCCTGACTC , CM000685.2:g.154380726_154380742delinsTCCCCTCGCCCTGACTC	GRCh38
NC_000023.10:g.153609086_153609102delinsTCCCCTCGCCCTGACTC , CM000685.1:g.153609086_153609102delinsTCCCCTCGCCCTGACTC	GRCh37
NC_000023.9:g.153262280_153262296delinsTCCCCTCGCCCTGACTC	NCBI36
NG_008677.1:g.11291_11307delinsTCCCCTCGCCCTGACTC , LRG_745:g.11291_11307delinsTCCCCTCGCCCTGACTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.400-27_400-11delinsTCCCCTCGCCCTGACTC	ENSP00000507245.1:n.400-27_400-11delinsTCCCCTCGCCCTGACTC
ENST00000682478.1:n.590-27_590-11delinsTCCCCTCGCCCTGACTC
ENST00000683576.1:n.590-27_590-11delinsTCCCCTCGCCCTGACTC
ENST00000683627.1:c.400-27_400-11delinsTCCCCTCGCCCTGACTC	ENSP00000507533.1:n.400-27_400-11delinsTCCCCTCGCCCTGACTC
ENST00000684082.1:c.357-27_357-11delinsTCCCCTCGCCCTGACTC	ENSP00000508266.1:n.357-27_357-11delinsTCCCCTCGCCCTGACTC
ENST00000684633.1:n.372-27_372-11delinsTCCCCTCGCCCTGACTC
ENST00000684678.1:c.396-27_396-11delinsTCCCCTCGCCCTGACTC	ENSP00000507059.1:n.396-27_396-11delinsTCCCCTCGCCCTGACTC
ENST00000369842.9:c.400-27_400-11delinsTCCCCTCGCCCTGACTC MANE Select	ENSP00000358857.4:n.400-27_400-11delinsTCCCCTCGCCCTGACTC
ENST00000369835.3:c.295-27_295-11delinsTCCCCTCGCCCTGACTC	ENSP00000358850.3:n.295-27_295-11delinsTCCCCTCGCCCTGACTC
ENST00000369842.8:c.400-27_400-11delinsTCCCCTCGCCCTGACTC	ENSP00000358857.4:n.400-27_400-11delinsTCCCCTCGCCCTGACTC
ENST00000428228.5:c.*305-27_*305-11delinsTCCCCTCGCCCTGACTC	ENSP00000401081.1:n.*305-27_*305-11delinsTCCCCTCGCCCTGACTC
ENST00000468294.5:n.360-27_360-11delinsTCCCCTCGCCCTGACTC
ENST00000471965.1:n.162_178delinsTCCCCTCGCCCTGACTC
ENST00000485261.1:n.590-27_590-11delinsTCCCCTCGCCCTGACTC
ENST00000486738.5:n.758-27_758-11delinsTCCCCTCGCCCTGACTC
ENST00000492448.1:n.383-27_383-11delinsTCCCCTCGCCCTGACTC
NM_000117.2:c.400-27_400-11delinsTCCCCTCGCCCTGACTC , LRG_745t1:c.400-27_400-11delinsTCCCCTCGCCCTGACTC	NP_000108.1:n.400-27_400-11delinsTCCCCTCGCCCTGACTC
XM_024452349.1:c.406-27_406-11delinsTCCCCTCGCCCTGACTC	XP_024308117.1:n.406-27_406-11delinsTCCCCTCGCCCTGACTC
NM_000117.3:c.400-27_400-11delinsTCCCCTCGCCCTGACTC MANE Select	NP_000108.1:n.400-27_400-11delinsTCCCCTCGCCCTGACTC