Canonical Allele Identifier: CA1403519299

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.134650922G= , CM000665.2:g.134650922G= GRCh38
NC_000003.11:g.134369764G= , CM000665.1:g.134369764G= GRCh37
NC_000003.10:g.135852454G= NCBI36
NG_054713.1:g.10132C=

Transcript Alleles

HGVS Amino-acid change
ENST00000423778.7:c.39C= (KY) MANE Select ENSP00000397598.2:p.Asp13=
ENST00000423778.6:c.39C= (KY) ENSP00000397598.2:p.Asp13=
ENST00000460895.5:c.-153+35484G= (EPHB1) ENSP00000417435.1:n.-153+35484G=
ENST00000467708.2:n.361+35484G= (EPHB1)
ENST00000503669.1:c.39C= (KY) ENSP00000426777.1:p.Asp13=
ENST00000506319.5:n.715C= (KY)
ENST00000508956.5:c.39C= (KY) ENSP00000421297.1:p.Asp13=
NM_178554.4:c.39C= (KY) NP_848649.3:p.Asp13=
XM_005247417.2:c.216C= (KY) XP_005247474.1:p.Asp72=
XM_005247418.2:c.216C= (KY) XP_005247475.1:p.Asp72=
XM_006713612.2:c.216C= (KY) XP_006713675.1:p.Asp72=
XR_241572.2:n.540-7762G=
XR_924521.1:n.540-22032G=
NM_001350859.1:c.39C= (KY) NP_001337788.1:p.Asp13=
NM_001350860.1:c.39C= (KY) NP_001337789.1:p.Asp13=
NM_001366276.1:c.39C= (KY) NP_001353205.1:p.Asp13=
NM_001366277.1:c.39C= (KY) NP_001353206.1:p.Asp13=
NM_178554.5:c.39C= (KY) NP_848649.3:p.Asp13=
XM_006713612.3:c.216C= (KY) XP_006713675.1:p.Asp72=
XM_017006287.1:c.216C= (KY) XP_016861776.1:p.Asp72=
XM_017006288.1:c.216C= (KY) XP_016861777.1:p.Asp72=
XM_017006290.1:c.216C= (KY) XP_016861779.1:p.Asp72=
XM_024453389.1:c.-153+35484G= (EPHB1) XP_024309157.1:n.-153+35484G=
XM_024453390.1:c.-153+35484G= (EPHB1) XP_024309158.1:n.-153+35484G=
XM_024453508.1:c.216C= (KY) XP_024309276.1:p.Asp72=
XR_002959586.1:n.1927+35484G= (CEP63)
NM_178554.6:c.39C= (KY) MANE Select NP_848649.3:p.Asp13=
NM_001350859.2:c.39C= (KY) NP_001337788.1:p.Asp13=
NM_001350860.2:c.39C= (KY) NP_001337789.1:p.Asp13=
NM_001366277.2:c.39C= (KY) NP_001353206.1:p.Asp13=