Canonical Allele Identifier: CA341381978
Gene: SNX7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.98695628C>G , CM000663.2:g.98695628C>G GRCh38
NC_000001.10:g.99161184C>G , CM000663.1:g.99161184C>G GRCh37
NC_000001.9:g.98933772C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306121.8:c.750C>G MANE Select ENSP00000304429.3:p.Phe250Leu
ENST00000306121.7:c.750C>G ENSP00000304429.3:p.Phe250Leu
ENST00000528824.1:c.*570C>G ENSP00000435172.1:n.*570C>G
ENST00000529992.5:c.585C>G ENSP00000434731.1:p.Phe195Leu
NM_015976.4:c.750C>G NP_057060.2:p.Phe250Leu
NM_152238.3:c.585C>G NP_689424.2:p.Phe195Leu
NR_033716.1:n.922C>G
XM_006710677.1:c.816C>G XP_006710740.1:p.Phe272Leu
XM_006710678.1:c.558C>G XP_006710741.1:p.Phe186Leu
XM_011541564.1:c.558C>G XP_011539866.1:p.Phe186Leu
NM_001364903.1:c.558C>G NP_001351832.1:p.Phe186Leu
XM_006710677.2:c.816C>G XP_006710740.1:p.Phe272Leu
XM_011541564.3:c.558C>G XP_011539866.1:p.Phe186Leu
XM_017001425.2:c.558C>G XP_016856914.1:p.Phe186Leu
XM_017001426.2:c.558C>G XP_016856915.1:p.Phe186Leu
XM_017001427.2:c.558C>G XP_016856916.1:p.Phe186Leu
XM_017001428.1:c.558C>G XP_016856917.1:p.Phe186Leu
NM_015976.5:c.750C>G MANE Select NP_057060.2:p.Phe250Leu
NM_152238.4:c.585C>G NP_689424.2:p.Phe195Leu
NR_033716.2:n.881C>G