Canonical Allele Identifier: CA2530696879

Gene: SLC30A3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27260222del , CM000664.2:g.27260222del	GRCh38
NC_000002.11:g.27483090del , CM000664.1:g.27483090del	GRCh37
NC_000002.10:g.27336594del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233535.9:c.96-1284del MANE Select	ENSP00000233535.4:n.96-1284del
ENST00000233535.8:c.96-1284del	ENSP00000233535.4:n.96-1284del
ENST00000424577.5:c.30-1284del	ENSP00000403959.1:n.30-1284del
ENST00000426569.1:c.-52-1284del	ENSP00000392673.1:n.-52-1284del
ENST00000426924.5:c.57-1284del	ENSP00000393545.1:n.57-1284del
ENST00000432351.5:c.-52-1284del	ENSP00000414320.1:n.-52-1284del
ENST00000445870.5:c.61-1284del
ENST00000450118.5:c.-41-1295del	ENSP00000403912.1:n.-41-1295del
NM_003459.4:c.96-1284del	NP_003450.2:n.96-1284del
XM_005264547.1:c.96-1284del	XP_005264604.1:n.96-1284del
XM_005264548.3:c.81-1284del	XP_005264605.1:n.81-1284del
XM_005264551.3:c.81-1284del	XP_005264608.1:n.81-1284del
XM_006712100.2:c.-53+215del	XP_006712163.1:n.-53+215del
XM_011533100.1:c.30-1284del	XP_011531402.1:n.30-1284del
XM_011533101.1:c.57-1284del	XP_011531403.1:n.57-1284del
XM_011533102.1:c.8-1284del	XP_011531404.1:n.8-1284del
XM_011533103.1:c.-116-1284del	XP_011531405.1:n.-116-1284del
NM_001318949.1:c.81-1284del	NP_001305878.1:n.81-1284del
NM_001318950.1:c.57-1284del	NP_001305879.1:n.57-1284del
NM_001318951.1:c.57-1284del	NP_001305880.1:n.57-1284del
XM_005264547.2:c.96-1284del	XP_005264604.1:n.96-1284del
XM_011533102.2:c.8-1284del	XP_011531404.1:n.8-1284del
XM_011533103.2:c.-116-1284del	XP_011531405.1:n.-116-1284del
XM_017004873.1:c.57-1284del	XP_016860362.1:n.57-1284del
XM_017004874.1:c.57-1284del	XP_016860363.1:n.57-1284del
XM_017004875.2:c.30-1284del	XP_016860364.1:n.30-1284del
NM_001318949.2:c.81-1284del	NP_001305878.1:n.81-1284del
NM_001318951.2:c.57-1284del	NP_001305880.1:n.57-1284del
NM_003459.5:c.96-1284del MANE Select	NP_003450.2:n.96-1284del
NM_001318950.2:c.57-1284del	NP_001305879.1:n.57-1284del