Canonical Allele Identifier: CA1860473332

Gene: SLC28A3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.84302386T= , CM000671.2:g.84302386T=	GRCh38
NC_000009.11:g.86917301T= , CM000671.1:g.86917301T=	GRCh37
NC_000009.10:g.86107121T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001199633.2:c.338A= MANE Select	NP_001186562.1:p.Tyr113=
ENST00000376238.5:c.338A= MANE Select	ENSP00000365413.4:p.Tyr113=
NM_001199633.1:c.338A=	NP_001186562.1:p.Tyr113=
NM_022127.2:c.338A=	NP_071410.1:p.Tyr113=
NM_022127.3:c.338A=	NP_071410.1:p.Tyr113=
NR_037638.2:n.660A=
NR_037638.3:n.639A=
ENST00000376238.4:c.338A=	ENSP00000365413.4:p.Tyr113=
XM_011518905.1:c.422A=	XP_011517207.1:p.Tyr141=
XM_011518905.2:c.422A=	XP_011517207.1:p.Tyr141=
XM_011518906.1:c.422A=	XP_011517208.1:p.Tyr141=
XM_011518906.2:c.422A=	XP_011517208.1:p.Tyr141=
XM_011518907.1:c.89A=	XP_011517209.1:p.Tyr30=
XM_011518907.2:c.89A=	XP_011517209.1:p.Tyr30=
XM_011518909.1:c.422A=	XP_011517211.1:p.Tyr141=
XM_011518909.2:c.422A=	XP_011517211.1:p.Tyr141=
XM_011518910.1:c.422A=	XP_011517212.1:p.Tyr141=
XM_011518910.2:c.422A=	XP_011517212.1:p.Tyr141=
XR_929832.1:n.549A=
XR_929832.2:n.554A=