Canonical Allele Identifier: CA1860470513

Gene: SLC28A3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.84290212A= , CM000671.2:g.84290212A=	GRCh38
NC_000009.11:g.86905127A= , CM000671.1:g.86905127A=	GRCh37
NC_000009.10:g.86094947A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000376238.5:c.1091T= MANE Select	ENSP00000365413.4:p.Met364=
ENST00000376238.4:c.1091T=	ENSP00000365413.4:p.Met364=
NM_001199633.1:c.1091T=	NP_001186562.1:p.Met364=
NM_022127.2:c.1091T=	NP_071410.1:p.Met364=
NR_037638.2:n.1413T=
XM_011518905.1:c.1175T=	XP_011517207.1:p.Met392=
XM_011518906.1:c.1175T=	XP_011517208.1:p.Met392=
XM_011518907.1:c.842T=	XP_011517209.1:p.Met281=
XM_011518908.1:c.452T=	XP_011517210.1:p.Met151=
XM_011518909.1:c.*184T=	XP_011517211.1:n.*184T=
XM_011518910.1:c.*108T=	XP_011517212.1:n.*108T=
XR_929832.1:n.1302T=
XM_011518905.2:c.1175T=	XP_011517207.1:p.Met392=
XM_011518906.2:c.1175T=	XP_011517208.1:p.Met392=
XM_011518907.2:c.842T=	XP_011517209.1:p.Met281=
XM_011518908.2:c.452T=	XP_011517210.1:p.Met151=
XM_011518909.2:c.*184T=	XP_011517211.1:n.*184T=
XM_011518910.2:c.*108T=	XP_011517212.1:n.*108T=
XR_929832.2:n.1307T=
NM_001199633.2:c.1091T= MANE Select	NP_001186562.1:p.Met364=
NM_022127.3:c.1091T=	NP_071410.1:p.Met364=
NR_037638.3:n.1392T=