Canonical Allele Identifier: CA2173753201

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711191G= , CM000677.2:g.44711191G=	GRCh38
NC_000015.9:g.45003389G= , CM000677.1:g.45003389G=	GRCh37
NC_000015.8:g.42790681G=	NCBI36
NG_012920.1:g.4705G=
NG_012920.2:g.4715G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-425C= MANE Select	ENSP00000508024.1:n.-425C=
ENST00000558573.1:n.126C=
XM_011521338.1:c.-425C=	XP_011519640.1:n.-425C=
XM_011521339.1:c.-306C=	XP_011519641.1:n.-306C=
XM_011521340.1:c.-247C=	XP_011519642.1:n.-247C=
XM_011521343.1:c.-509C=	XP_011519645.1:n.-509C=
XM_011521345.1:c.-480C=	XP_011519647.1:n.-480C=
XM_011521338.3:c.-425C=	XP_011519640.1:n.-425C=
XM_011521339.3:c.-306C=	XP_011519641.1:n.-306C=
XM_011521340.3:c.-247C=	XP_011519642.1:n.-247C=
XM_011521343.3:c.-509C=	XP_011519645.1:n.-509C=
XM_011521345.3:c.-480C=	XP_011519647.1:n.-480C=
NM_001387260.1:c.-76+141C=	NP_001374189.1:n.-76+141C=
NM_001387261.1:c.-247C=	NP_001374190.1:n.-247C=
NM_001387262.1:c.-515C=	NP_001374191.1:n.-515C=
NM_001387263.1:c.-425C= MANE Select	NP_001374192.1:n.-425C=