Canonical Allele Identifier: CA1126200679

Gene: SLC28A3

Linked Data

• gnomAD v3: 9-84307020-AGCTTCGTGTGATGGC-A
• gnomAD v4: 9-84307020-AGCTTCGTGTGATGGC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.84307021_84307035del , CM000671.2:g.84307021_84307035del	GRCh38
NC_000009.11:g.86921936_86921950del , CM000671.1:g.86921936_86921950del	GRCh37
NC_000009.10:g.86111756_86111770del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000376238.5:c.243-1690_243-1676del MANE Select	ENSP00000365413.4:n.243-1690_243-1676del
ENST00000376238.4:c.243-1690_243-1676del	ENSP00000365413.4:n.243-1690_243-1676del
ENST00000495823.1:n.445-1690_445-1676del
NM_001199633.1:c.243-1690_243-1676del	NP_001186562.1:n.243-1690_243-1676del
NM_022127.2:c.243-1690_243-1676del	NP_071410.1:n.243-1690_243-1676del
NR_037638.2:n.565-1690_565-1676del
XM_011518905.1:c.418+2594_418+2608del	XP_011517207.1:n.418+2594_418+2608del
XM_011518906.1:c.418+2594_418+2608del	XP_011517208.1:n.418+2594_418+2608del
XM_011518907.1:c.85+2594_85+2608del	XP_011517209.1:n.85+2594_85+2608del
XM_011518909.1:c.418+2594_418+2608del	XP_011517211.1:n.418+2594_418+2608del
XM_011518910.1:c.418+2594_418+2608del	XP_011517212.1:n.418+2594_418+2608del
XR_929832.1:n.545+2594_545+2608del
XM_011518905.2:c.418+2594_418+2608del	XP_011517207.1:n.418+2594_418+2608del
XM_011518906.2:c.418+2594_418+2608del	XP_011517208.1:n.418+2594_418+2608del
XM_011518907.2:c.85+2594_85+2608del	XP_011517209.1:n.85+2594_85+2608del
XM_011518909.2:c.418+2594_418+2608del	XP_011517211.1:n.418+2594_418+2608del
XM_011518910.2:c.418+2594_418+2608del	XP_011517212.1:n.418+2594_418+2608del
XR_929832.2:n.550+2594_550+2608del
NM_001199633.2:c.243-1690_243-1676del MANE Select	NP_001186562.1:n.243-1690_243-1676del
NM_022127.3:c.243-1690_243-1676del	NP_071410.1:n.243-1690_243-1676del
NR_037638.3:n.544-1690_544-1676del