Canonical Allele Identifier: CA1165617201

Gene: SZT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43439025C= , CM000663.2:g.43439025C=	GRCh38
NC_000001.10:g.43904696C= , CM000663.1:g.43904696C=	GRCh37
NC_000001.9:g.43677283C=	NCBI36
NG_029091.1:g.54141C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000562955.2:c.6553C=	ENSP00000457168.1:p.Arg2185=
ENST00000634258.3:c.6724C= MANE Select	ENSP00000489255.1:p.Arg2242=
ENST00000648058.1:n.3178C=
ENST00000649403.1:n.1474C=
ENST00000471177.1:n.387C=
ENST00000562955.1:c.6553C=	ENSP00000457168.1:p.Arg2185=
ENST00000634258.1:c.6724C=	ENSP00000489255.1:p.Arg2242=
NM_015284.3:c.6553C=	NP_056099.3:p.Arg2185=
XM_005270686.2:c.6787C=	XP_005270743.1:p.Arg2263=
XM_006710501.2:c.6724C=	XP_006710564.1:p.Arg2242=
XM_011541103.1:c.6841C=	XP_011539405.1:p.Arg2281=
XM_011541104.1:c.6670C=	XP_011539406.1:p.Arg2224=
XM_011541105.1:c.6667C=	XP_011539407.1:p.Arg2223=
XM_011541106.1:c.6667C=	XP_011539408.1:p.Arg2223=
XM_011541107.1:c.6268C=	XP_011539409.1:p.Arg2090=
NM_001365999.1:c.6724C= MANE Select	NP_001352928.1:p.Arg2242=
XM_005270686.3:c.6787C=	XP_005270743.1:p.Arg2263=
XM_011541106.3:c.6667C=	XP_011539408.1:p.Arg2223=
XM_011541107.2:c.6268C=	XP_011539409.1:p.Arg2090=
XM_017000819.1:c.6634C=	XP_016856308.1:p.Arg2212=
XM_017000820.1:c.6616C=	XP_016856309.1:p.Arg2206=
XM_017000821.1:c.5416C=	XP_016856310.1:p.Arg1806=
XR_001737075.1:n.6870C=
XR_002956151.1:n.6870C=
NM_015284.4:c.6553C=	NP_056099.3:p.Arg2185=