Canonical Allele Identifier: CA1126200589

Gene: SLC28A3

Linked Data

• dbSNP Id: rs150442323
• gnomAD v3: 9-84306994-CAAAAAAAAA-C
• gnomAD v4: 9-84306994-CAAAAAAAAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.84307012_84307020del , CM000671.2:g.84307012_84307020del	GRCh38
NC_000009.11:g.86921927_86921935del , CM000671.1:g.86921927_86921935del	GRCh37
NC_000009.10:g.86111747_86111755del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000376238.5:c.243-1658_243-1650del MANE Select	ENSP00000365413.4:n.243-1658_243-1650del
ENST00000376238.4:c.243-1658_243-1650del	ENSP00000365413.4:n.243-1658_243-1650del
ENST00000495823.1:n.445-1658_445-1650del
NM_001199633.1:c.243-1658_243-1650del	NP_001186562.1:n.243-1658_243-1650del
NM_022127.2:c.243-1658_243-1650del	NP_071410.1:n.243-1658_243-1650del
NR_037638.2:n.565-1658_565-1650del
XM_011518905.1:c.418+2626_418+2634del	XP_011517207.1:n.418+2626_418+2634del
XM_011518906.1:c.418+2626_418+2634del	XP_011517208.1:n.418+2626_418+2634del
XM_011518907.1:c.85+2626_85+2634del	XP_011517209.1:n.85+2626_85+2634del
XM_011518909.1:c.418+2626_418+2634del	XP_011517211.1:n.418+2626_418+2634del
XM_011518910.1:c.418+2626_418+2634del	XP_011517212.1:n.418+2626_418+2634del
XR_929832.1:n.545+2626_545+2634del
XM_011518905.2:c.418+2626_418+2634del	XP_011517207.1:n.418+2626_418+2634del
XM_011518906.2:c.418+2626_418+2634del	XP_011517208.1:n.418+2626_418+2634del
XM_011518907.2:c.85+2626_85+2634del	XP_011517209.1:n.85+2626_85+2634del
XM_011518909.2:c.418+2626_418+2634del	XP_011517211.1:n.418+2626_418+2634del
XM_011518910.2:c.418+2626_418+2634del	XP_011517212.1:n.418+2626_418+2634del
XR_929832.2:n.550+2626_550+2634del
NM_001199633.2:c.243-1658_243-1650del MANE Select	NP_001186562.1:n.243-1658_243-1650del
NM_022127.3:c.243-1658_243-1650del	NP_071410.1:n.243-1658_243-1650del
NR_037638.3:n.544-1658_544-1650del