Canonical Allele Identifier: CA2518605340

Gene: SLC28A3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.84306825_84306836del , CM000671.2:g.84306825_84306836del	GRCh38
NC_000009.11:g.86921740_86921751del , CM000671.1:g.86921740_86921751del	GRCh37
NC_000009.10:g.86111560_86111571del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376238.5:c.243-1490_243-1479del MANE Select	ENSP00000365413.4:n.243-1490_243-1479del
ENST00000376238.4:c.243-1490_243-1479del	ENSP00000365413.4:n.243-1490_243-1479del
ENST00000495823.1:n.445-1490_445-1479del
NM_001199633.1:c.243-1490_243-1479del	NP_001186562.1:n.243-1490_243-1479del
NM_022127.2:c.243-1490_243-1479del	NP_071410.1:n.243-1490_243-1479del
NR_037638.2:n.565-1490_565-1479del
XM_011518905.1:c.418+2794_418+2805del	XP_011517207.1:n.418+2794_418+2805del
XM_011518906.1:c.418+2794_418+2805del	XP_011517208.1:n.418+2794_418+2805del
XM_011518907.1:c.85+2794_85+2805del	XP_011517209.1:n.85+2794_85+2805del
XM_011518909.1:c.418+2794_418+2805del	XP_011517211.1:n.418+2794_418+2805del
XM_011518910.1:c.418+2794_418+2805del	XP_011517212.1:n.418+2794_418+2805del
XR_929832.1:n.545+2794_545+2805del
XM_011518905.2:c.418+2794_418+2805del	XP_011517207.1:n.418+2794_418+2805del
XM_011518906.2:c.418+2794_418+2805del	XP_011517208.1:n.418+2794_418+2805del
XM_011518907.2:c.85+2794_85+2805del	XP_011517209.1:n.85+2794_85+2805del
XM_011518909.2:c.418+2794_418+2805del	XP_011517211.1:n.418+2794_418+2805del
XM_011518910.2:c.418+2794_418+2805del	XP_011517212.1:n.418+2794_418+2805del
XR_929832.2:n.550+2794_550+2805del
NM_001199633.2:c.243-1490_243-1479del MANE Select	NP_001186562.1:n.243-1490_243-1479del
NM_022127.3:c.243-1490_243-1479del	NP_071410.1:n.243-1490_243-1479del
NR_037638.3:n.544-1490_544-1479del