Canonical Allele Identifier: CA1860477387

Gene: SLC28A3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.84307031A= , CM000671.2:g.84307031A=	GRCh38
NC_000009.11:g.86921946A= , CM000671.1:g.86921946A=	GRCh37
NC_000009.10:g.86111766A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000376238.5:c.243-1686T= MANE Select	ENSP00000365413.4:n.243-1686T=
ENST00000376238.4:c.243-1686T=	ENSP00000365413.4:n.243-1686T=
ENST00000495823.1:n.445-1686T=
NM_001199633.1:c.243-1686T=	NP_001186562.1:n.243-1686T=
NM_022127.2:c.243-1686T=	NP_071410.1:n.243-1686T=
NR_037638.2:n.565-1686T=
XM_011518905.1:c.418+2598T=	XP_011517207.1:n.418+2598T=
XM_011518906.1:c.418+2598T=	XP_011517208.1:n.418+2598T=
XM_011518907.1:c.85+2598T=	XP_011517209.1:n.85+2598T=
XM_011518909.1:c.418+2598T=	XP_011517211.1:n.418+2598T=
XM_011518910.1:c.418+2598T=	XP_011517212.1:n.418+2598T=
XR_929832.1:n.545+2598T=
XM_011518905.2:c.418+2598T=	XP_011517207.1:n.418+2598T=
XM_011518906.2:c.418+2598T=	XP_011517208.1:n.418+2598T=
XM_011518907.2:c.85+2598T=	XP_011517209.1:n.85+2598T=
XM_011518909.2:c.418+2598T=	XP_011517211.1:n.418+2598T=
XM_011518910.2:c.418+2598T=	XP_011517212.1:n.418+2598T=
XR_929832.2:n.550+2598T=
NM_001199633.2:c.243-1686T= MANE Select	NP_001186562.1:n.243-1686T=
NM_022127.3:c.243-1686T=	NP_071410.1:n.243-1686T=
NR_037638.3:n.544-1686T=