Canonical Allele Identifier: CA354624017

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.134650917A>T , CM000665.2:g.134650917A>T GRCh38
NC_000003.11:g.134369759A>T , CM000665.1:g.134369759A>T GRCh37
NC_000003.10:g.135852449A>T NCBI36
NG_054713.1:g.10137T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000423778.7:c.44T>A (KY) MANE Select ENSP00000397598.2:p.Leu15Gln
ENST00000423778.6:c.44T>A (KY) ENSP00000397598.2:p.Leu15Gln
ENST00000460895.5:c.-153+35479A>T (EPHB1) ENSP00000417435.1:n.-153+35479A>T
ENST00000467708.2:n.361+35479A>T (EPHB1)
ENST00000503669.1:c.44T>A (KY) ENSP00000426777.1:p.Leu15Gln
ENST00000506319.5:n.720T>A (KY)
ENST00000508956.5:c.44T>A (KY) ENSP00000421297.1:p.Leu15Gln
NM_178554.4:c.44T>A (KY) NP_848649.3:p.Leu15Gln
XM_005247417.2:c.221T>A (KY) XP_005247474.1:p.Leu74Gln
XM_005247418.2:c.221T>A (KY) XP_005247475.1:p.Leu74Gln
XM_006713612.2:c.221T>A (KY) XP_006713675.1:p.Leu74Gln
XR_241572.2:n.540-7767A>T
XR_924521.1:n.540-22037A>T
NM_001350859.1:c.44T>A (KY) NP_001337788.1:p.Leu15Gln
NM_001350860.1:c.44T>A (KY) NP_001337789.1:p.Leu15Gln
NM_001366276.1:c.44T>A (KY) NP_001353205.1:p.Leu15Gln
NM_001366277.1:c.44T>A (KY) NP_001353206.1:p.Leu15Gln
NM_178554.5:c.44T>A (KY) NP_848649.3:p.Leu15Gln
XM_006713612.3:c.221T>A (KY) XP_006713675.1:p.Leu74Gln
XM_017006287.1:c.221T>A (KY) XP_016861776.1:p.Leu74Gln
XM_017006288.1:c.221T>A (KY) XP_016861777.1:p.Leu74Gln
XM_017006290.1:c.221T>A (KY) XP_016861779.1:p.Leu74Gln
XM_024453389.1:c.-153+35479A>T (EPHB1) XP_024309157.1:n.-153+35479A>T
XM_024453390.1:c.-153+35479A>T (EPHB1) XP_024309158.1:n.-153+35479A>T
XM_024453508.1:c.221T>A (KY) XP_024309276.1:p.Leu74Gln
XR_002959586.1:n.1927+35479A>T (CEP63)
NM_178554.6:c.44T>A (KY) MANE Select NP_848649.3:p.Leu15Gln
NM_001350859.2:c.44T>A (KY) NP_001337788.1:p.Leu15Gln
NM_001350860.2:c.44T>A (KY) NP_001337789.1:p.Leu15Gln
NM_001366277.2:c.44T>A (KY) NP_001353206.1:p.Leu15Gln