Canonical Allele Identifier: CA1860487995

Gene: SLC28A3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.84329486A= , CM000671.2:g.84329486A=	GRCh38
NC_000009.11:g.86944401A= , CM000671.1:g.86944401A=	GRCh37
NC_000009.10:g.86134221A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376238.5:c.60+11088T= MANE Select	ENSP00000365413.4:n.60+11088T=
ENST00000376238.4:c.60+11088T=	ENSP00000365413.4:n.60+11088T=
ENST00000495823.1:n.86+11088T=
NM_001199633.1:c.60+11088T=	NP_001186562.1:n.60+11088T=
NM_022127.2:c.60+11088T=	NP_071410.1:n.60+11088T=
NR_037638.2:n.206+11088T=
XM_011518905.1:c.60+11088T=	XP_011517207.1:n.60+11088T=
XM_011518906.1:c.60+11088T=	XP_011517208.1:n.60+11088T=
XM_011518907.1:c.-97-16032T=	XP_011517209.1:n.-97-16032T=
XM_011518909.1:c.60+11088T=	XP_011517211.1:n.60+11088T=
XM_011518910.1:c.60+11088T=	XP_011517212.1:n.60+11088T=
XR_929832.1:n.187+11088T=
XM_011518905.2:c.60+11088T=	XP_011517207.1:n.60+11088T=
XM_011518906.2:c.60+11088T=	XP_011517208.1:n.60+11088T=
XM_011518907.2:c.-97-16032T=	XP_011517209.1:n.-97-16032T=
XM_011518909.2:c.60+11088T=	XP_011517211.1:n.60+11088T=
XM_011518910.2:c.60+11088T=	XP_011517212.1:n.60+11088T=
XR_929832.2:n.192+11088T=
NM_001199633.2:c.60+11088T= MANE Select	NP_001186562.1:n.60+11088T=
NM_022127.3:c.60+11088T=	NP_071410.1:n.60+11088T=
NR_037638.3:n.185+11088T=