Canonical Allele Identifier: CA2841739398

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44669495G>T , CM000677.2:g.44669495G>T	GRCh38
NC_000015.9:g.44961693G>T , CM000677.1:g.44961693G>T	GRCh37
NC_000015.8:g.42748985G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.930+15C>A MANE Select	ENSP00000508024.1:n.930+15C>A
ENST00000434130.6:c.930+15C>A	ENSP00000416673.1:n.930+15C>A
ENST00000434130.5:c.930+15C>A	ENSP00000416673.1:n.930+15C>A
ENST00000560775.5:c.930+15C>A	ENSP00000453915.1:n.930+15C>A
ENST00000560780.1:c.363+15C>A	ENSP00000453695.1:n.363+15C>A
NM_001145112.1:c.930+15C>A	NP_001138584.1:n.930+15C>A
XM_005254224.2:c.930+15C>A	XP_005254281.1:n.930+15C>A
XM_011521336.1:c.930+15C>A	XP_011519638.1:n.930+15C>A
XM_011521337.1:c.921+15C>A	XP_011519639.1:n.921+15C>A
XM_011521338.1:c.930+15C>A	XP_011519640.1:n.930+15C>A
XM_011521339.1:c.930+15C>A	XP_011519641.1:n.930+15C>A
XM_011521340.1:c.930+15C>A	XP_011519642.1:n.930+15C>A
XM_011521341.1:c.930+15C>A	XP_011519643.1:n.930+15C>A
XM_011521342.1:c.708+15C>A	XP_011519644.1:n.708+15C>A
XM_011521343.1:c.678+15C>A	XP_011519645.1:n.678+15C>A
XM_011521344.1:c.678+15C>A	XP_011519646.1:n.678+15C>A
XM_011521345.1:c.669+15C>A	XP_011519647.1:n.669+15C>A
XM_011521346.1:c.495+15C>A	XP_011519648.1:n.495+15C>A
XM_011521347.1:c.363+15C>A	XP_011519649.1:n.363+15C>A
XM_011521348.1:c.363+15C>A	XP_011519650.1:n.363+15C>A
NM_001330283.1:c.363+15C>A	NP_001317212.1:n.363+15C>A
XM_011521336.2:c.1044+15C>A	XP_011519638.2:n.1044+15C>A
XM_011521337.2:c.1035+15C>A	XP_011519639.2:n.1035+15C>A
XM_011521338.3:c.930+15C>A	XP_011519640.1:n.930+15C>A
XM_011521339.3:c.930+15C>A	XP_011519641.1:n.930+15C>A
XM_011521340.3:c.930+15C>A	XP_011519642.1:n.930+15C>A
XM_011521342.2:c.708+15C>A	XP_011519644.1:n.708+15C>A
XM_011521343.3:c.678+15C>A	XP_011519645.1:n.678+15C>A
XM_011521344.3:c.678+15C>A	XP_011519646.1:n.678+15C>A
XM_011521345.3:c.669+15C>A	XP_011519647.1:n.669+15C>A
XM_011521346.2:c.609+15C>A	XP_011519648.2:n.609+15C>A
XM_017022000.2:c.1044+15C>A	XP_016877489.1:n.1044+15C>A
XM_017022001.2:c.669+15C>A	XP_016877490.1:n.669+15C>A
NM_001145112.2:c.930+15C>A	NP_001138584.1:n.930+15C>A
NM_001330283.2:c.363+15C>A	NP_001317212.1:n.363+15C>A
NM_001387260.1:c.837+15C>A	NP_001374189.1:n.837+15C>A
NM_001387261.1:c.930+15C>A	NP_001374190.1:n.930+15C>A
NM_001387262.1:c.930+15C>A	NP_001374191.1:n.930+15C>A
NM_001387263.1:c.930+15C>A MANE Select	NP_001374192.1:n.930+15C>A
NM_001387264.1:c.837+15C>A	NP_001374193.1:n.837+15C>A