Canonical Allele Identifier: CA15131213
Gene: SNX7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.98711697G>A , CM000663.2:g.98711697G>A GRCh38
NC_000001.10:g.99177253G>A , CM000663.1:g.99177253G>A GRCh37
NC_000001.9:g.98949841G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306121.8:c.1125+9794G>A MANE Select ENSP00000304429.3:n.1125+9794G>A
ENST00000306121.7:c.1125+9794G>A ENSP00000304429.3:n.1125+9794G>A
ENST00000528824.1:c.*945+9794G>A ENSP00000435172.1:n.*945+9794G>A
ENST00000529992.5:c.960+9794G>A ENSP00000434731.1:n.960+9794G>A
NM_015976.4:c.1125+9794G>A NP_057060.2:n.1125+9794G>A
NM_152238.3:c.960+9794G>A NP_689424.2:n.960+9794G>A
NR_033716.1:n.1297+9794G>A
XM_006710677.1:c.1191+9794G>A XP_006710740.1:n.1191+9794G>A
XM_006710678.1:c.933+9794G>A XP_006710741.1:n.933+9794G>A
XM_011541564.1:c.933+9794G>A XP_011539866.1:n.933+9794G>A
NM_001364903.1:c.933+9794G>A NP_001351832.1:n.933+9794G>A
XM_006710677.2:c.1191+9794G>A XP_006710740.1:n.1191+9794G>A
XM_011541564.3:c.933+9794G>A XP_011539866.1:n.933+9794G>A
XM_017001425.2:c.933+9794G>A XP_016856914.1:n.933+9794G>A
XM_017001426.2:c.933+9794G>A XP_016856915.1:n.933+9794G>A
XM_017001427.2:c.933+9794G>A XP_016856916.1:n.933+9794G>A
XM_017001428.1:c.933+9794G>A XP_016856917.1:n.933+9794G>A
NM_015976.5:c.1125+9794G>A MANE Select NP_057060.2:n.1125+9794G>A
NM_152238.4:c.960+9794G>A NP_689424.2:n.960+9794G>A
NR_033716.2:n.1256+9794G>A
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