Canonical Allele Identifier: CA2567183445

Gene: SLC28A3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.84307015_84307016insG , CM000671.2:g.84307015_84307016insG	GRCh38
NC_000009.11:g.86921930_86921931insG , CM000671.1:g.86921930_86921931insG	GRCh37
NC_000009.10:g.86111750_86111751insG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376238.5:c.243-1671_243-1670insC MANE Select	ENSP00000365413.4:n.243-1671_243-1670insC
ENST00000376238.4:c.243-1671_243-1670insC	ENSP00000365413.4:n.243-1671_243-1670insC
ENST00000495823.1:n.445-1671_445-1670insC
NM_001199633.1:c.243-1671_243-1670insC	NP_001186562.1:n.243-1671_243-1670insC
NM_022127.2:c.243-1671_243-1670insC	NP_071410.1:n.243-1671_243-1670insC
NR_037638.2:n.565-1671_565-1670insC
XM_011518905.1:c.418+2613_418+2614insC	XP_011517207.1:n.418+2613_418+2614insC
XM_011518906.1:c.418+2613_418+2614insC	XP_011517208.1:n.418+2613_418+2614insC
XM_011518907.1:c.85+2613_85+2614insC	XP_011517209.1:n.85+2613_85+2614insC
XM_011518909.1:c.418+2613_418+2614insC	XP_011517211.1:n.418+2613_418+2614insC
XM_011518910.1:c.418+2613_418+2614insC	XP_011517212.1:n.418+2613_418+2614insC
XR_929832.1:n.545+2613_545+2614insC
XM_011518905.2:c.418+2613_418+2614insC	XP_011517207.1:n.418+2613_418+2614insC
XM_011518906.2:c.418+2613_418+2614insC	XP_011517208.1:n.418+2613_418+2614insC
XM_011518907.2:c.85+2613_85+2614insC	XP_011517209.1:n.85+2613_85+2614insC
XM_011518909.2:c.418+2613_418+2614insC	XP_011517211.1:n.418+2613_418+2614insC
XM_011518910.2:c.418+2613_418+2614insC	XP_011517212.1:n.418+2613_418+2614insC
XR_929832.2:n.550+2613_550+2614insC
NM_001199633.2:c.243-1671_243-1670insC MANE Select	NP_001186562.1:n.243-1671_243-1670insC
NM_022127.3:c.243-1671_243-1670insC	NP_071410.1:n.243-1671_243-1670insC
NR_037638.3:n.544-1671_544-1670insC