Canonical Allele Identifier: CA767360565

Gene: SLC30A3

Linked Data

• dbSNP Id: rs1285553280
• MyVariant Identifiers: chr2:g.27483107_27483108del (hg19) ; chr2:g.27260239_27260240del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27260242_27260243del , CM000664.2:g.27260242_27260243del	GRCh38
NC_000002.11:g.27483110_27483111del , CM000664.1:g.27483110_27483111del	GRCh37
NC_000002.10:g.27336614_27336615del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233535.9:c.96-1306_96-1305del MANE Select	ENSP00000233535.4:n.96-1306_96-1305del
ENST00000233535.8:c.96-1306_96-1305del	ENSP00000233535.4:n.96-1306_96-1305del
ENST00000424577.5:c.30-1306_30-1305del	ENSP00000403959.1:n.30-1306_30-1305del
ENST00000426569.1:c.-52-1306_-52-1305del	ENSP00000392673.1:n.-52-1306_-52-1305del
ENST00000426924.5:c.57-1306_57-1305del	ENSP00000393545.1:n.57-1306_57-1305del
ENST00000432351.5:c.-52-1306_-52-1305del	ENSP00000414320.1:n.-52-1306_-52-1305del
ENST00000445870.5:c.61-1306_61-1305del
ENST00000450118.5:c.-41-1317_-41-1316del	ENSP00000403912.1:n.-41-1317_-41-1316del
NM_003459.4:c.96-1306_96-1305del	NP_003450.2:n.96-1306_96-1305del
XM_005264547.1:c.96-1306_96-1305del	XP_005264604.1:n.96-1306_96-1305del
XM_005264548.3:c.81-1306_81-1305del	XP_005264605.1:n.81-1306_81-1305del
XM_005264551.3:c.81-1306_81-1305del	XP_005264608.1:n.81-1306_81-1305del
XM_006712100.2:c.-53+193_-53+194del	XP_006712163.1:n.-53+193_-53+194del
XM_011533100.1:c.30-1306_30-1305del	XP_011531402.1:n.30-1306_30-1305del
XM_011533101.1:c.57-1306_57-1305del	XP_011531403.1:n.57-1306_57-1305del
XM_011533102.1:c.8-1306_8-1305del	XP_011531404.1:n.8-1306_8-1305del
XM_011533103.1:c.-116-1306_-116-1305del	XP_011531405.1:n.-116-1306_-116-1305del
NM_001318949.1:c.81-1306_81-1305del	NP_001305878.1:n.81-1306_81-1305del
NM_001318950.1:c.57-1306_57-1305del	NP_001305879.1:n.57-1306_57-1305del
NM_001318951.1:c.57-1306_57-1305del	NP_001305880.1:n.57-1306_57-1305del
XM_005264547.2:c.96-1306_96-1305del	XP_005264604.1:n.96-1306_96-1305del
XM_011533102.2:c.8-1306_8-1305del	XP_011531404.1:n.8-1306_8-1305del
XM_011533103.2:c.-116-1306_-116-1305del	XP_011531405.1:n.-116-1306_-116-1305del
XM_017004873.1:c.57-1306_57-1305del	XP_016860362.1:n.57-1306_57-1305del
XM_017004874.1:c.57-1306_57-1305del	XP_016860363.1:n.57-1306_57-1305del
XM_017004875.2:c.30-1306_30-1305del	XP_016860364.1:n.30-1306_30-1305del
NM_001318949.2:c.81-1306_81-1305del	NP_001305878.1:n.81-1306_81-1305del
NM_001318951.2:c.57-1306_57-1305del	NP_001305880.1:n.57-1306_57-1305del
NM_003459.5:c.96-1306_96-1305del MANE Select	NP_003450.2:n.96-1306_96-1305del
NM_001318950.2:c.57-1306_57-1305del	NP_001305879.1:n.57-1306_57-1305del