Canonical Allele Identifier: CA341969730

Gene: SNX27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151683422T>C , CM000663.2:g.151683422T>C	GRCh38
NC_000001.10:g.151655898T>C , CM000663.1:g.151655898T>C	GRCh37
NC_000001.9:g.149922522T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368838.2:c.813T>C
ENST00000368841.7:c.*887T>C	ENSP00000357834.2:n.*887T>C
ENST00000368843.8:c.1216T>C	ENSP00000357836.3:p.Tyr406His
ENST00000458013.7:c.1216T>C MANE Select	ENSP00000400333.2:p.Tyr406His
ENST00000642349.1:c.950T>C	ENSP00000494331.1:n.950T>C
ENST00000642376.1:c.853T>C	ENSP00000496645.1:p.Tyr285His
ENST00000642479.1:c.*594T>C	ENSP00000496775.1:n.*594T>C
ENST00000643179.1:n.1024T>C
ENST00000643937.1:n.894T>C
ENST00000644113.1:n.900T>C
ENST00000644970.1:n.1214T>C
ENST00000647328.1:n.937T>C
ENST00000647551.1:n.4665T>C
ENST00000368838.1:c.937T>C	ENSP00000357831.1:p.Tyr313His
ENST00000368841.6:c.*887T>C	ENSP00000357834.2:n.*887T>C
ENST00000368843.7:c.1216T>C	ENSP00000357836.3:p.Tyr406His
ENST00000458013.6:c.1216T>C	ENSP00000400333.2:p.Tyr406His
NM_030918.5:c.1216T>C	NP_112180.4:p.Tyr406His
XM_005245509.1:c.1216T>C	XP_005245566.1:p.Tyr406His
XM_005245510.2:c.907T>C	XP_005245567.1:p.Tyr303His
XM_005245511.3:c.658T>C	XP_005245568.1:p.Tyr220His
XM_011510024.1:c.913T>C	XP_011508326.1:p.Tyr305His
XM_011510025.1:c.853T>C	XP_011508327.1:p.Tyr285His
NM_001330723.1:c.1216T>C	NP_001317652.1:p.Tyr406His
XM_005245510.3:c.907T>C	XP_005245567.1:p.Tyr303His
XM_005245511.4:c.658T>C	XP_005245568.1:p.Tyr220His
XM_011510024.2:c.913T>C	XP_011508326.1:p.Tyr305His
XM_011510025.2:c.853T>C	XP_011508327.1:p.Tyr285His
XM_017002417.1:c.853T>C	XP_016857906.1:p.Tyr285His
XM_024450038.1:c.658T>C	XP_024305806.1:p.Tyr220His
XM_024450039.1:c.658T>C	XP_024305807.1:p.Tyr220His
NM_001330723.2:c.1216T>C MANE Select	NP_001317652.1:p.Tyr406His
NM_030918.6:c.1216T>C	NP_112180.4:p.Tyr406His