Canonical Allele Identifier: CA1165610899

Gene: SZT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43420983G= , CM000663.2:g.43420983G=	GRCh38
NC_000001.10:g.43886654G= , CM000663.1:g.43886654G=	GRCh37
NC_000001.9:g.43659241G=	NCBI36
NG_029091.1:g.36099G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000562955.2:c.1496G=	ENSP00000457168.1:p.Ser499=
ENST00000634258.3:c.1496G= MANE Select	ENSP00000489255.1:p.Ser499=
ENST00000639852.1:c.1162G=	ENSP00000492385.1:n.1162G=
ENST00000470139.1:n.227G=
ENST00000562955.1:c.1496G=	ENSP00000457168.1:p.Ser499=
ENST00000634258.1:c.1496G=	ENSP00000489255.1:p.Ser499=
NM_015284.3:c.1496G=	NP_056099.3:p.Ser499=
XM_005270686.2:c.1559G=	XP_005270743.1:p.Ser520=
XM_006710501.2:c.1496G=	XP_006710564.1:p.Ser499=
XM_011541103.1:c.1613G=	XP_011539405.1:p.Ser538=
XM_011541104.1:c.1442G=	XP_011539406.1:p.Ser481=
XM_011541105.1:c.1439G=	XP_011539407.1:p.Ser480=
XM_011541106.1:c.1439G=	XP_011539408.1:p.Ser480=
XM_011541107.1:c.1040G=	XP_011539409.1:p.Ser347=
NM_001365999.1:c.1496G= MANE Select	NP_001352928.1:p.Ser499=
XM_005270686.3:c.1559G=	XP_005270743.1:p.Ser520=
XM_011541106.3:c.1439G=	XP_011539408.1:p.Ser480=
XM_011541107.2:c.1040G=	XP_011539409.1:p.Ser347=
XM_017000819.1:c.1559G=	XP_016856308.1:p.Ser520=
XM_017000820.1:c.1388G=	XP_016856309.1:p.Ser463=
XM_017000821.1:c.188G=	XP_016856310.1:p.Ser63=
XR_001737075.1:n.1642G=
XR_001737076.1:n.1644G=
XR_001737077.1:n.1644G=
XR_002956151.1:n.1642G=
NM_015284.4:c.1496G=	NP_056099.3:p.Ser499=