Canonical Allele Identifier: CA1093500
Community Standard Title: NM_001330723.2(SNX27):c.802-4C>T
Gene: SNX27 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.151662162C>T , CM000663.2:g.151662162C>T GRCh38
NC_000001.10:g.151634638C>T , CM000663.1:g.151634638C>T GRCh37
NC_000001.9:g.149901262C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001330723.2:c.802-4C>T MANE Select NP_001317652.1:n.802-4C>T
ENST00000458013.7:c.802-4C>T MANE Select ENSP00000400333.2:n.802-4C>T
NM_001330723.1:c.802-4C>T NP_001317652.1:n.802-4C>T
NM_030918.5:c.802-4C>T NP_112180.4:n.802-4C>T
NM_030918.6:c.802-4C>T NP_112180.4:n.802-4C>T
ENST00000368838.1:c.523-4C>T ENSP00000357831.1:n.523-4C>T
ENST00000368838.2:c.399-4C>T
ENST00000368841.6:c.*473-4C>T ENSP00000357834.2:n.*473-4C>T
ENST00000368841.7:c.*473-4C>T ENSP00000357834.2:n.*473-4C>T
ENST00000368843.7:c.802-4C>T ENSP00000357836.3:n.802-4C>T
ENST00000368843.8:c.802-4C>T ENSP00000357836.3:n.802-4C>T
ENST00000458013.6:c.802-4C>T ENSP00000400333.2:n.802-4C>T
ENST00000482791.2:c.125-4C>T
ENST00000642349.1:c.536-4C>T ENSP00000494331.1:n.536-4C>T
ENST00000642376.1:c.439-4C>T ENSP00000496645.1:n.439-4C>T
ENST00000642479.1:c.*180-4C>T ENSP00000496775.1:n.*180-4C>T
ENST00000643179.1:n.610-4C>T
ENST00000643814.1:n.523-4C>T
ENST00000643937.1:n.480-4C>T
ENST00000644113.1:n.486-4C>T
ENST00000644970.1:n.800-4C>T
ENST00000647328.1:n.523-4C>T
ENST00000647454.1:n.251-4C>T
XM_005245509.1:c.802-4C>T XP_005245566.1:n.802-4C>T
XM_005245510.2:c.493-4C>T XP_005245567.1:n.493-4C>T
XM_005245510.3:c.493-4C>T XP_005245567.1:n.493-4C>T
XM_005245511.3:c.244-4C>T XP_005245568.1:n.244-4C>T
XM_005245511.4:c.244-4C>T XP_005245568.1:n.244-4C>T
XM_011510024.1:c.499-4C>T XP_011508326.1:n.499-4C>T
XM_011510024.2:c.499-4C>T XP_011508326.1:n.499-4C>T
XM_011510025.1:c.439-4C>T XP_011508327.1:n.439-4C>T
XM_011510025.2:c.439-4C>T XP_011508327.1:n.439-4C>T
XM_011510026.1:c.802-4C>T XP_011508328.1:n.802-4C>T
XM_011510026.2:c.802-4C>T XP_011508328.1:n.802-4C>T
XM_017002417.1:c.439-4C>T XP_016857906.1:n.439-4C>T
XM_024450038.1:c.244-4C>T XP_024305806.1:n.244-4C>T
XM_024450039.1:c.244-4C>T XP_024305807.1:n.244-4C>T