Canonical Allele Identifier: CA1144228779

Gene: SZT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43403222C= , CM000663.2:g.43403222C=	GRCh38
NC_000001.10:g.43868893C= , CM000663.1:g.43868893C=	GRCh37
NC_000001.9:g.43641480C=	NCBI36
NG_029091.1:g.18338C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357658.4:n.91C=
ENST00000406439.7:c.73C=	ENSP00000386070.2:p.Arg25=
ENST00000562955.2:c.73C=	ENSP00000457168.1:p.Arg25=
ENST00000634258.3:c.73C= MANE Select	ENSP00000489255.1:p.Arg25=
ENST00000638631.1:n.143C=
ENST00000357658.3:n.137C=
ENST00000372450.8:c.73C=	ENSP00000361528.4:p.Arg25=
ENST00000406439.6:c.73C=	ENSP00000386070.2:p.Arg25=
ENST00000562955.1:c.73C=	ENSP00000457168.1:p.Arg25=
ENST00000634258.1:c.73C=	ENSP00000489255.1:p.Arg25=
NM_015284.3:c.73C=	NP_056099.3:p.Arg25=
XM_005270686.2:c.136C=	XP_005270743.1:p.Arg46=
XM_006710501.2:c.73C=	XP_006710564.1:p.Arg25=
XM_011541103.1:c.190C=	XP_011539405.1:p.Arg64=
XM_011541104.1:c.190C=	XP_011539406.1:p.Arg64=
XM_011541105.1:c.16C=	XP_011539407.1:p.Arg6=
XM_011541106.1:c.16C=	XP_011539408.1:p.Arg6=
NM_001365999.1:c.73C= MANE Select	NP_001352928.1:p.Arg25=
XM_005270686.3:c.136C=	XP_005270743.1:p.Arg46=
XM_011541106.3:c.16C=	XP_011539408.1:p.Arg6=
XM_017000819.1:c.136C=	XP_016856308.1:p.Arg46=
XM_017000820.1:c.136C=	XP_016856309.1:p.Arg46=
XR_001737075.1:n.219C=
XR_001737076.1:n.221C=
XR_001737077.1:n.221C=
XR_002956151.1:n.219C=
NM_015284.4:c.73C=	NP_056099.3:p.Arg25=