Canonical Allele Identifier: CA435827882

Gene: KY EPHB1 CEP63

Linked Data

• gnomAD v4: 3-134650916-C-T
• MyVariant Identifiers: chr3:g.134369758C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.134650916C>T , CM000665.2:g.134650916C>T	GRCh38
NC_000003.11:g.134369758C>T , CM000665.1:g.134369758C>T	GRCh37
NC_000003.10:g.135852448C>T	NCBI36
NG_054713.1:g.10138G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000423778.7:c.45G>A (KY) MANE Select	ENSP00000397598.2:p.Leu15=
ENST00000423778.6:c.45G>A (KY)	ENSP00000397598.2:p.Leu15=
ENST00000460895.5:c.-153+35478C>T (EPHB1)	ENSP00000417435.1:n.-153+35478C>T
ENST00000467708.2:n.361+35478C>T (EPHB1)
ENST00000503669.1:c.45G>A (KY)	ENSP00000426777.1:p.Leu15=
ENST00000506319.5:n.721G>A (KY)
ENST00000508956.5:c.45G>A (KY)	ENSP00000421297.1:p.Leu15=
NM_178554.4:c.45G>A (KY)	NP_848649.3:p.Leu15=
XM_005247417.2:c.222G>A (KY)	XP_005247474.1:p.Leu74=
XM_005247418.2:c.222G>A (KY)	XP_005247475.1:p.Leu74=
XM_006713612.2:c.222G>A (KY)	XP_006713675.1:p.Leu74=
XR_241572.2:n.540-7768C>T
XR_924521.1:n.540-22038C>T
NM_001350859.1:c.45G>A (KY)	NP_001337788.1:p.Leu15=
NM_001350860.1:c.45G>A (KY)	NP_001337789.1:p.Leu15=
NM_001366276.1:c.45G>A (KY)	NP_001353205.1:p.Leu15=
NM_001366277.1:c.45G>A (KY)	NP_001353206.1:p.Leu15=
NM_178554.5:c.45G>A (KY)	NP_848649.3:p.Leu15=
XM_006713612.3:c.222G>A (KY)	XP_006713675.1:p.Leu74=
XM_017006287.1:c.222G>A (KY)	XP_016861776.1:p.Leu74=
XM_017006288.1:c.222G>A (KY)	XP_016861777.1:p.Leu74=
XM_017006290.1:c.222G>A (KY)	XP_016861779.1:p.Leu74=
XM_024453389.1:c.-153+35478C>T (EPHB1)	XP_024309157.1:n.-153+35478C>T
XM_024453390.1:c.-153+35478C>T (EPHB1)	XP_024309158.1:n.-153+35478C>T
XM_024453508.1:c.222G>A (KY)	XP_024309276.1:p.Leu74=
XR_002959586.1:n.1927+35478C>T (CEP63)
NM_178554.6:c.45G>A (KY) MANE Select	NP_848649.3:p.Leu15=
NM_001350859.2:c.45G>A (KY)	NP_001337788.1:p.Leu15=
NM_001350860.2:c.45G>A (KY)	NP_001337789.1:p.Leu15=
NM_001366277.2:c.45G>A (KY)	NP_001353206.1:p.Leu15=