Canonical Allele Identifier: CA1165612479

Gene: SZT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43424324C= , CM000663.2:g.43424324C=	GRCh38
NC_000001.10:g.43889995C= , CM000663.1:g.43889995C=	GRCh37
NC_000001.9:g.43662582C=	NCBI36
NG_029091.1:g.39440C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000562955.2:c.2363C=	ENSP00000457168.1:p.Ser788=
ENST00000634258.3:c.2363C= MANE Select	ENSP00000489255.1:p.Ser788=
ENST00000470139.1:n.1094C=
ENST00000562955.1:c.2363C=	ENSP00000457168.1:p.Ser788=
ENST00000634258.1:c.2363C=	ENSP00000489255.1:p.Ser788=
NM_015284.3:c.2363C=	NP_056099.3:p.Ser788=
XM_005270686.2:c.2426C=	XP_005270743.1:p.Ser809=
XM_006710501.2:c.2363C=	XP_006710564.1:p.Ser788=
XM_011541103.1:c.2480C=	XP_011539405.1:p.Ser827=
XM_011541104.1:c.2309C=	XP_011539406.1:p.Ser770=
XM_011541105.1:c.2306C=	XP_011539407.1:p.Ser769=
XM_011541106.1:c.2306C=	XP_011539408.1:p.Ser769=
XM_011541107.1:c.1907C=	XP_011539409.1:p.Ser636=
NM_001365999.1:c.2363C= MANE Select	NP_001352928.1:p.Ser788=
XM_005270686.3:c.2426C=	XP_005270743.1:p.Ser809=
XM_011541106.3:c.2306C=	XP_011539408.1:p.Ser769=
XM_011541107.2:c.1907C=	XP_011539409.1:p.Ser636=
XM_017000819.1:c.2426C=	XP_016856308.1:p.Ser809=
XM_017000820.1:c.2255C=	XP_016856309.1:p.Ser752=
XM_017000821.1:c.1055C=	XP_016856310.1:p.Ser352=
XR_001737075.1:n.2509C=
XR_001737076.1:n.2511C=
XR_001737077.1:n.2511C=
XR_002956151.1:n.2509C=
NM_015284.4:c.2363C=	NP_056099.3:p.Ser788=