Canonical Allele Identifier: CA613315566
Gene: SLC7A7 HGNC NCBI

Linked Data

dbSNP Id: rs1315366056

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22775543_22775544del , CM000676.2:g.22775543_22775544del GRCh38
NC_000014.8:g.23244752_23244753del , CM000676.1:g.23244752_23244753del GRCh37
NC_000014.7:g.22314592_22314593del NCBI36
NG_012851.2:g.59278_59279del , LRG_695:g.59278_59279del

Transcript Alleles

HGVS Amino-acid change
ENST00000555911.2:c.999-3_999-2del ENSP00000452551.2:n.999-3_999-2del
ENST00000698939.1:c.*65-3_*65-2del ENSP00000514047.1:n.*65-3_*65-2del
ENST00000698940.1:n.61-3_61-2del
ENST00000397532.9:c.999-3_999-2del ENSP00000380666.4:n.999-3_999-2del
ENST00000674313.1:c.999-3_999-2del MANE Select ENSP00000501493.1:n.999-3_999-2del
ENST00000285850.11:c.999-3_999-2del ENSP00000285850.7:n.999-3_999-2del
ENST00000397528.8:c.999-3_999-2del ENSP00000380662.4:n.999-3_999-2del
ENST00000397529.6:c.999-3_999-2del ENSP00000380663.2:n.999-3_999-2del
ENST00000397532.7:c.999-3_999-2del ENSP00000380666.3:n.999-3_999-2del
ENST00000554061.5:n.670-3_670-2del
ENST00000554517.5:c.201-3_201-2del ENSP00000452083.1:n.201-3_201-2del
ENST00000555678.1:n.257_258del
ENST00000555702.5:c.999-3_999-2del ENSP00000451881.1:n.999-3_999-2del
ENST00000556287.5:c.895-3_895-2del ENSP00000450715.1:n.895-3_895-2del
ENST00000556350.1:c.143-3_143-2del
NM_001126105.2:c.999-3_999-2del , LRG_695t1:c.999-3_999-2del NP_001119577.1:n.999-3_999-2del
NM_001126106.2:c.999-3_999-2del , LRG_695t2:c.999-3_999-2del NP_001119578.1:n.999-3_999-2del
NR_040448.1:n.1614-3_1614-2del
XM_006720302.1:c.999-3_999-2del XP_006720365.1:n.999-3_999-2del
XM_011537298.1:c.999-3_999-2del XP_011535600.1:n.999-3_999-2del
XM_011537299.1:c.999-3_999-2del XP_011535601.1:n.999-3_999-2del
XM_006720302.2:c.999-3_999-2del XP_006720365.1:n.999-3_999-2del
XM_011537298.3:c.999-3_999-2del XP_011535600.1:n.999-3_999-2del
NM_001126105.3:c.999-3_999-2del NP_001119577.1:n.999-3_999-2del
NM_001126106.4:c.999-3_999-2del NP_001119578.1:n.999-3_999-2del
NM_003982.4:c.999-3_999-2del MANE Select NP_003973.3:n.999-3_999-2del