Canonical Allele Identifier: CA1860477358

Gene: SLC28A3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.84307020_84307021delinsAG , CM000671.2:g.84307020_84307021delinsAG	GRCh38
NC_000009.11:g.86921935_86921936delinsAG , CM000671.1:g.86921935_86921936delinsAG	GRCh37
NC_000009.10:g.86111755_86111756delinsAG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000376238.5:c.243-1676_243-1675delinsCT MANE Select	ENSP00000365413.4:n.243-1676_243-1675deli...
ENST00000376238.4:c.243-1676_243-1675delinsCT	ENSP00000365413.4:n.243-1676_243-1675deli...
ENST00000495823.1:n.445-1676_445-1675delinsCT
NM_001199633.1:c.243-1676_243-1675delinsCT	NP_001186562.1:n.243-1676_243-1675delinsC...
NM_022127.2:c.243-1676_243-1675delinsCT	NP_071410.1:n.243-1676_243-1675delinsCT
NR_037638.2:n.565-1676_565-1675delinsCT
XM_011518905.1:c.418+2608_418+2609delinsCT	XP_011517207.1:n.418+2608_418+2609delinsC...
XM_011518906.1:c.418+2608_418+2609delinsCT	XP_011517208.1:n.418+2608_418+2609delinsC...
XM_011518907.1:c.85+2608_85+2609delinsCT	XP_011517209.1:n.85+2608_85+2609delinsCT
XM_011518909.1:c.418+2608_418+2609delinsCT	XP_011517211.1:n.418+2608_418+2609delinsC...
XM_011518910.1:c.418+2608_418+2609delinsCT	XP_011517212.1:n.418+2608_418+2609delinsC...
XR_929832.1:n.545+2608_545+2609delinsCT
XM_011518905.2:c.418+2608_418+2609delinsCT	XP_011517207.1:n.418+2608_418+2609delinsC...
XM_011518906.2:c.418+2608_418+2609delinsCT	XP_011517208.1:n.418+2608_418+2609delinsC...
XM_011518907.2:c.85+2608_85+2609delinsCT	XP_011517209.1:n.85+2608_85+2609delinsCT
XM_011518909.2:c.418+2608_418+2609delinsCT	XP_011517211.1:n.418+2608_418+2609delinsC...
XM_011518910.2:c.418+2608_418+2609delinsCT	XP_011517212.1:n.418+2608_418+2609delinsC...
XR_929832.2:n.550+2608_550+2609delinsCT
NM_001199633.2:c.243-1676_243-1675delinsCT MANE Select	NP_001186562.1:n.243-1676_243-1675delinsC...
NM_022127.3:c.243-1676_243-1675delinsCT	NP_071410.1:n.243-1676_243-1675delinsCT
NR_037638.3:n.544-1676_544-1675delinsCT