Canonical Allele Identifier: CA1860480790

Gene: SLC28A3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.84313419T= , CM000671.2:g.84313419T=	GRCh38
NC_000009.11:g.86928334T= , CM000671.1:g.86928334T=	GRCh37
NC_000009.10:g.86118154T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376238.5:c.96A= MANE Select	ENSP00000365413.4:p.Ser32=
ENST00000376238.4:c.96A=	ENSP00000365413.4:p.Ser32=
ENST00000495823.1:n.122A=
NM_001199633.1:c.96A=	NP_001186562.1:p.Ser32=
NM_022127.2:c.96A=	NP_071410.1:p.Ser32=
NR_037638.2:n.242A=
XM_011518905.1:c.96A=	XP_011517207.1:p.Ser32=
XM_011518906.1:c.96A=	XP_011517208.1:p.Ser32=
XM_011518907.1:c.-62A=	XP_011517209.1:n.-62A=
XM_011518909.1:c.96A=	XP_011517211.1:p.Ser32=
XM_011518910.1:c.96A=	XP_011517212.1:p.Ser32=
XR_929832.1:n.223A=
XM_011518905.2:c.96A=	XP_011517207.1:p.Ser32=
XM_011518906.2:c.96A=	XP_011517208.1:p.Ser32=
XM_011518907.2:c.-62A=	XP_011517209.1:n.-62A=
XM_011518909.2:c.96A=	XP_011517211.1:p.Ser32=
XM_011518910.2:c.96A=	XP_011517212.1:p.Ser32=
XR_929832.2:n.228A=
NM_001199633.2:c.96A= MANE Select	NP_001186562.1:p.Ser32=
NM_022127.3:c.96A=	NP_071410.1:p.Ser32=
NR_037638.3:n.221A=