Canonical Allele Identifier: CA83751960

Gene: KY EPHB1 CEP63

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.134603375C>G , CM000665.2:g.134603375C>G	GRCh38
NC_000003.11:g.134322217C>G , CM000665.1:g.134322217C>G	GRCh37
NC_000003.10:g.135804907C>G	NCBI36
NG_054713.1:g.57679G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_178554.6:c.*204G>C (KY) MANE Select	NP_848649.3:n.*204G>C
ENST00000423778.7:c.*204G>C (KY) MANE Select	ENSP00000397598.2:n.*204G>C
NM_001350859.1:c.*204G>C (KY)	NP_001337788.1:n.*204G>C
NM_001350859.2:c.*204G>C (KY)	NP_001337788.1:n.*204G>C
NM_001366276.1:c.*204G>C (KY)	NP_001353205.1:n.*204G>C
NM_178554.4:c.*204G>C (KY)	NP_848649.3:n.*204G>C
NM_178554.5:c.*204G>C (KY)	NP_848649.3:n.*204G>C
ENST00000423778.6:c.*204G>C (KY)	ENSP00000397598.2:n.*204G>C
ENST00000467708.2:n.106+5391C>G (EPHB1)
ENST00000472904.5:n.161+5391C>G (EPHB1)
ENST00000508956.5:c.*204G>C (KY)	ENSP00000421297.1:n.*204G>C
XM_005247417.2:c.*204G>C (KY)	XP_005247474.1:n.*204G>C
XM_005247418.2:c.*204G>C (KY)	XP_005247475.1:n.*204G>C
XM_006713612.2:c.*204G>C (KY)	XP_006713675.1:n.*204G>C
XM_006713612.3:c.*204G>C (KY)	XP_006713675.1:n.*204G>C
XM_011512747.1:c.*204G>C (KY)	XP_011511049.1:n.*204G>C
XM_017006287.1:c.*204G>C (KY)	XP_016861776.1:n.*204G>C
XM_017006288.1:c.*204G>C (KY)	XP_016861777.1:n.*204G>C
XM_017006290.1:c.*204G>C (KY)	XP_016861779.1:n.*204G>C
XM_024453389.1:c.-408+5391C>G (EPHB1)	XP_024309157.1:n.-408+5391C>G
XM_024453390.1:c.-408+2175C>G (EPHB1)	XP_024309158.1:n.-408+2175C>G
XR_002959586.1:n.1672+5391C>G (CEP63)
XR_002959589.1:n.1567+5391C>G (CEP63)
XR_241572.2:n.284+5391C>G
XR_427411.2:n.284+5391C>G
XR_924521.1:n.284+5391C>G