Canonical Allele Identifier: CA1144228778

Gene: SZT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43423153C= , CM000663.2:g.43423153C=	GRCh38
NC_000001.10:g.43888824C= , CM000663.1:g.43888824C=	GRCh37
NC_000001.9:g.43661411C=	NCBI36
NG_029091.1:g.38269C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000562955.2:c.2092C=	ENSP00000457168.1:p.Gln698=
ENST00000634258.3:c.2092C= MANE Select	ENSP00000489255.1:p.Gln698=
ENST00000470139.1:n.823C=
ENST00000562955.1:c.2092C=	ENSP00000457168.1:p.Gln698=
ENST00000634258.1:c.2092C=	ENSP00000489255.1:p.Gln698=
NM_015284.3:c.2092C=	NP_056099.3:p.Gln698=
XM_005270686.2:c.2155C=	XP_005270743.1:p.Gln719=
XM_006710501.2:c.2092C=	XP_006710564.1:p.Gln698=
XM_011541103.1:c.2209C=	XP_011539405.1:p.Gln737=
XM_011541104.1:c.2038C=	XP_011539406.1:p.Gln680=
XM_011541105.1:c.2035C=	XP_011539407.1:p.Gln679=
XM_011541106.1:c.2035C=	XP_011539408.1:p.Gln679=
XM_011541107.1:c.1636C=	XP_011539409.1:p.Gln546=
NM_001365999.1:c.2092C= MANE Select	NP_001352928.1:p.Gln698=
XM_005270686.3:c.2155C=	XP_005270743.1:p.Gln719=
XM_011541106.3:c.2035C=	XP_011539408.1:p.Gln679=
XM_011541107.2:c.1636C=	XP_011539409.1:p.Gln546=
XM_017000819.1:c.2155C=	XP_016856308.1:p.Gln719=
XM_017000820.1:c.1984C=	XP_016856309.1:p.Gln662=
XM_017000821.1:c.784C=	XP_016856310.1:p.Gln262=
XR_001737075.1:n.2238C=
XR_001737076.1:n.2240C=
XR_001737077.1:n.2240C=
XR_002956151.1:n.2238C=
NM_015284.4:c.2092C=	NP_056099.3:p.Gln698=