Canonical Allele Identifier: CA1772801077

Gene: PTK2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27373302A= , CM000670.2:g.27373302A=	GRCh38
NC_000008.10:g.27230819A= , CM000670.1:g.27230819A=	GRCh37
NC_000008.9:g.27286736A=	NCBI36
NG_029510.1:g.66821A=
NG_029510.2:g.66821A=

Transcript Alleles

HGVS	Amino-acid Change
NM_173176.3:c.-37-24246A= MANE Select	NP_775268.1:n.-37-24246A=
ENST00000346049.10:c.-37-24246A= MANE Select	ENSP00000332816.6:n.-37-24246A=
NM_004103.4:c.-37-24246A=	NP_004094.3:n.-37-24246A=
NM_173174.2:c.-37-24246A=	NP_775266.1:n.-37-24246A=
NM_173174.3:c.-37-24246A=	NP_775266.1:n.-37-24246A=
NM_173175.2:c.-37-24246A=	NP_775267.1:n.-37-24246A=
NM_173176.2:c.-37-24246A=	NP_775268.1:n.-37-24246A=
ENST00000346049.9:c.-37-24246A=	ENSP00000332816.6:n.-37-24246A=
ENST00000397501.5:c.-37-24246A=	ENSP00000380638.1:n.-37-24246A=
ENST00000420218.3:c.-37-24246A=	ENSP00000391995.2:n.-37-24246A=
ENST00000521164.5:c.-37-24246A=	ENSP00000430404.1:n.-37-24246A=
ENST00000522338.5:c.-37-24246A=	ENSP00000429694.1:n.-37-24246A=
ENST00000522517.5:c.-37-24246A=	ENSP00000428271.1:n.-37-24246A=
XM_005273448.3:c.-37-24246A=	XP_005273505.1:n.-37-24246A=
XM_005273448.5:c.-37-24246A=	XP_005273505.1:n.-37-24246A=
XM_011544441.1:c.-37-24246A=	XP_011542743.1:n.-37-24246A=
XM_011544441.2:c.-37-24246A=	XP_011542743.1:n.-37-24246A=
XM_011544442.1:c.-37-24246A=	XP_011542744.1:n.-37-24246A=
XM_011544442.3:c.-37-24246A=	XP_011542744.1:n.-37-24246A=
XM_017013214.1:c.-37-24246A=	XP_016868703.1:n.-37-24246A=
XM_017013215.1:c.-37-24246A=	XP_016868704.1:n.-37-24246A=
XM_017013216.2:c.-37-24246A=	XP_016868705.1:n.-37-24246A=