Canonical Allele Identifier: CA351342077

Gene: PASK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.241115383C>A , CM000664.2:g.241115383C>A	GRCh38
NC_000002.11:g.242054798C>A , CM000664.1:g.242054798C>A	GRCh37
NC_000002.10:g.241703471C>A	NCBI36
NG_052850.1:g.39965G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234040.9:c.3103G>T MANE Select	ENSP00000234040.5:p.Val1035Phe
ENST00000234040.8:c.3103G>T	ENSP00000234040.4:p.Val1035Phe
ENST00000358649.8:c.3103G>T	ENSP00000351475.4:p.Val1035Phe
ENST00000403638.7:c.3103G>T	ENSP00000384438.3:p.Val1035Phe
ENST00000405260.5:c.3103G>T	ENSP00000384016.1:p.Val1035Phe
ENST00000493544.1:n.3536G>T
ENST00000544142.5:c.3103G>T	ENSP00000441374.2:p.Val1035Phe
NM_001252119.1:c.3103G>T	NP_001239048.1:p.Val1035Phe
NM_001252120.1:c.3103G>T	NP_001239049.1:p.Val1035Phe
NM_001252122.1:c.2998G>T	NP_001239051.1:p.Val1000Phe
NM_001252124.1:c.3103G>T	NP_001239053.1:p.Val1035Phe
NM_015148.3:c.3103G>T	NP_055963.2:p.Val1035Phe
XM_005246991.1:c.2455G>T	XP_005247048.1:p.Val819Phe
XM_011510826.1:c.3178G>T	XP_011509128.1:p.Val1060Phe
XM_011510827.1:c.3178G>T	XP_011509129.1:p.Val1060Phe
XM_011510828.1:c.3103G>T	XP_011509130.1:p.Val1035Phe
XM_011510829.1:c.3103G>T	XP_011509131.1:p.Val1035Phe
XM_011510830.1:c.3103G>T	XP_011509132.1:p.Val1035Phe
XM_011510831.1:c.2545G>T	XP_011509133.1:p.Val849Phe
XM_011510832.1:c.2545G>T	XP_011509134.1:p.Val849Phe
XM_011510833.1:c.2455G>T	XP_011509135.1:p.Val819Phe
XM_011510834.1:c.1945G>T	XP_011509136.1:p.Val649Phe
XM_011510835.1:c.1732G>T	XP_011509137.1:p.Val578Phe
XR_922893.1:n.3208G>T
XM_011510829.2:c.3103G>T	XP_011509131.1:p.Val1035Phe
XM_011510830.2:c.3103G>T	XP_011509132.1:p.Val1035Phe
XM_011510831.2:c.2545G>T	XP_011509133.1:p.Val849Phe
XM_011510832.2:c.2545G>T	XP_011509134.1:p.Val849Phe
XM_017003635.1:c.3103G>T	XP_016859124.1:p.Val1035Phe
XM_017003636.1:c.3103G>T	XP_016859125.1:p.Val1035Phe
XR_001738678.2:n.3228G>T
NM_001252119.2:c.3103G>T	NP_001239048.1:p.Val1035Phe
NM_001252122.2:c.2998G>T	NP_001239051.1:p.Val1000Phe
NM_001252124.2:c.3103G>T	NP_001239053.1:p.Val1035Phe
NM_015148.4:c.3103G>T MANE Select	NP_055963.2:p.Val1035Phe
NM_001252120.2:c.3103G>T	NP_001239049.1:p.Val1035Phe