Canonical Allele Identifier: CA2173753226

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711291C= , CM000677.2:g.44711291C=	GRCh38
NC_000015.9:g.45003489C= , CM000677.1:g.45003489C=	GRCh37
NC_000015.8:g.42790781C=	NCBI36
NG_012920.1:g.4805C=
NG_012920.2:g.4815C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-525G= MANE Select	ENSP00000508024.1:n.-525G=
ENST00000558573.1:n.26G=
XM_011521338.1:c.-525G=	XP_011519640.1:n.-525G=
XM_011521339.1:c.-406G=	XP_011519641.1:n.-406G=
XM_011521340.1:c.-347G=	XP_011519642.1:n.-347G=
XM_011521343.1:c.-609G=	XP_011519645.1:n.-609G=
XM_011521345.1:c.-580G=	XP_011519647.1:n.-580G=
XM_011521338.3:c.-525G=	XP_011519640.1:n.-525G=
XM_011521339.3:c.-406G=	XP_011519641.1:n.-406G=
XM_011521340.3:c.-347G=	XP_011519642.1:n.-347G=
XM_011521343.3:c.-609G=	XP_011519645.1:n.-609G=
XM_011521345.3:c.-580G=	XP_011519647.1:n.-580G=
NM_001387260.1:c.-76+41G=	NP_001374189.1:n.-76+41G=
NM_001387261.1:c.-347G=	NP_001374190.1:n.-347G=
NM_001387262.1:c.-615G=	NP_001374191.1:n.-615G=
NM_001387263.1:c.-525G= MANE Select	NP_001374192.1:n.-525G=