Canonical Allele Identifier: CA12719917
Gene: PTK2B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.27337604T>C , CM000670.2:g.27337604T>C GRCh38
NC_000008.10:g.27195121T>C , CM000670.1:g.27195121T>C GRCh37
NC_000008.9:g.27251038T>C NCBI36
NG_029510.1:g.31123T>C
NG_029510.2:g.31123T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000346049.10:c.-38+11923T>C MANE Select ENSP00000332816.6:n.-38+11923T>C
ENST00000346049.9:c.-38+11923T>C ENSP00000332816.6:n.-38+11923T>C
ENST00000397501.5:c.-38+11923T>C ENSP00000380638.1:n.-38+11923T>C
ENST00000420218.3:c.-38+11923T>C ENSP00000391995.2:n.-38+11923T>C
ENST00000521164.5:c.-38+11923T>C ENSP00000430404.1:n.-38+11923T>C
ENST00000522338.5:c.-38+11923T>C ENSP00000429694.1:n.-38+11923T>C
ENST00000522517.5:c.-38+10721T>C ENSP00000428271.1:n.-38+10721T>C
NM_004103.4:c.-38+11923T>C NP_004094.3:n.-38+11923T>C
NM_173174.2:c.-38+11923T>C NP_775266.1:n.-38+11923T>C
NM_173175.2:c.-38+11923T>C NP_775267.1:n.-38+11923T>C
NM_173176.2:c.-38+11923T>C NP_775268.1:n.-38+11923T>C
XM_005273448.3:c.-38+11923T>C XP_005273505.1:n.-38+11923T>C
XM_011544441.1:c.-38+10721T>C XP_011542743.1:n.-38+10721T>C
XM_011544442.1:c.-38+11923T>C XP_011542744.1:n.-38+11923T>C
XM_005273448.5:c.-38+11923T>C XP_005273505.1:n.-38+11923T>C
XM_011544441.2:c.-38+10721T>C XP_011542743.1:n.-38+10721T>C
XM_011544442.3:c.-38+11923T>C XP_011542744.1:n.-38+11923T>C
XM_017013214.1:c.-38+11923T>C XP_016868703.1:n.-38+11923T>C
XM_017013215.1:c.-38+10721T>C XP_016868704.1:n.-38+10721T>C
XM_017013216.2:c.-38+11923T>C XP_016868705.1:n.-38+11923T>C
NM_173176.3:c.-38+11923T>C MANE Select NP_775268.1:n.-38+11923T>C
NM_173174.3:c.-38+11923T>C NP_775266.1:n.-38+11923T>C
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