Canonical Allele Identifier: CA340548506

Gene: PATJ

Linked Data

• dbSNP Id: rs1189532402
• MyVariant Identifiers: chr1:g.62380319C>T (hg19) ; chr1:g.61914647C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.61914647C>T , CM000663.2:g.61914647C>T	GRCh38
NC_000001.10:g.62380319C>T , CM000663.1:g.62380319C>T	GRCh37
NC_000001.9:g.62152907C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642238.2:c.3553C>T MANE Select	ENSP00000494277.1:p.Gln1185Ter
ENST00000316485.11:c.3491-3377C>T	ENSP00000326199.7:n.3491-3377C>T
ENST00000371158.6:c.3553C>T	ENSP00000360200.2:p.Gln1185Ter
ENST00000459752.5:n.3667C>T
ENST00000484562.5:n.3667C>T
ENST00000484937.5:c.1930C>T	ENSP00000433669.1:p.Gln644Ter
ENST00000490547.2:c.1C>T	ENSP00000489475.1:p.Gln1Ter
ENST00000494842.2:c.89C>T
ENST00000613764.4:c.3381+13188C>T	ENSP00000479041.1:n.3381+13188C>T
ENST00000635023.1:c.*1521C>T	ENSP00000489335.1:n.*1521C>T
ENST00000635214.1:n.3667C>T
NM_176877.2:c.3553C>T	NP_795352.2:p.Gln1185Ter
XM_005270341.2:c.3553C>T	XP_005270398.1:p.Gln1185Ter
XM_005270347.1:c.3553C>T	XP_005270404.1:p.Gln1185Ter
XM_006710278.2:c.3553C>T	XP_006710341.1:p.Gln1185Ter
XM_011540462.1:c.3553C>T	XP_011538764.1:p.Gln1185Ter
XM_011540463.1:c.3553C>T	XP_011538765.1:p.Gln1185Ter
XM_011540464.1:c.3553C>T	XP_011538766.1:p.Gln1185Ter
XM_011540465.1:c.3553C>T	XP_011538767.1:p.Gln1185Ter
XM_011540466.1:c.3553C>T	XP_011538768.1:p.Gln1185Ter
XM_011540467.1:c.3553C>T	XP_011538769.1:p.Gln1185Ter
XM_011540468.1:c.3553C>T	XP_011538770.1:p.Gln1185Ter
XM_011540469.1:c.3553C>T	XP_011538771.1:p.Gln1185Ter
NM_001350145.1:c.3553C>T	NP_001337074.1:p.Gln1185Ter
NM_176877.3:c.3553C>T	NP_795352.2:p.Gln1185Ter
XM_005270347.2:c.3553C>T	XP_005270404.1:p.Gln1185Ter
XM_006710278.4:c.3553C>T	XP_006710341.1:p.Gln1185Ter
XM_011540462.3:c.3553C>T	XP_011538764.1:p.Gln1185Ter
XM_011540463.2:c.3553C>T	XP_011538765.1:p.Gln1185Ter
XM_011540464.3:c.3553C>T	XP_011538766.1:p.Gln1185Ter
XM_011540465.3:c.3553C>T	XP_011538767.1:p.Gln1185Ter
XM_011540466.3:c.3553C>T	XP_011538768.1:p.Gln1185Ter
XM_011540467.3:c.3553C>T	XP_011538769.1:p.Gln1185Ter
XM_011540468.3:c.3553C>T	XP_011538770.1:p.Gln1185Ter
XM_011540469.3:c.3553C>T	XP_011538771.1:p.Gln1185Ter
XM_016999998.2:c.3553C>T	XP_016855487.1:p.Gln1185Ter
XM_016999999.2:c.3553C>T	XP_016855488.1:p.Gln1185Ter
XM_017000000.1:c.2644C>T	XP_016855489.1:p.Gln882Ter
XM_017000001.1:c.718C>T	XP_016855490.1:p.Gln240Ter
XM_024448614.1:c.3553C>T	XP_024304382.1:p.Gln1185Ter
XM_024448642.1:c.3553C>T	XP_024304410.1:p.Gln1185Ter
XR_001736900.2:n.3667C>T
XR_002957157.1:n.3667C>T
NM_001350145.3:c.3553C>T MANE Select	NP_001337074.2:p.Gln1185Ter
NM_176877.5:c.3553C>T	NP_795352.3:p.Gln1185Ter