Canonical Allele Identifier: CA341972200

Gene: SNX27

Linked Data

• MyVariant Identifiers: chr1:g.151664995G>T (hg19) ; chr1:g.151692519G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151692519G>T , CM000663.2:g.151692519G>T	GRCh38
NC_000001.10:g.151664995G>T , CM000663.1:g.151664995G>T	GRCh37
NC_000001.9:g.149931619G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000368838.2:c.921G>T
ENST00000368841.7:c.*995G>T	ENSP00000357834.2:n.*995G>T
ENST00000368843.8:c.1324G>T	ENSP00000357836.3:p.Val442Phe
ENST00000458013.7:c.1324G>T MANE Select	ENSP00000400333.2:p.Val442Phe
ENST00000642349.1:c.1058G>T	ENSP00000494331.1:n.1058G>T
ENST00000642376.1:c.961G>T	ENSP00000496645.1:p.Val321Phe
ENST00000642479.1:c.*702G>T	ENSP00000496775.1:n.*702G>T
ENST00000643179.1:n.1132G>T
ENST00000643937.1:n.1002G>T
ENST00000644970.1:n.1322G>T
ENST00000647328.1:n.1045G>T
ENST00000647551.1:n.4773G>T
ENST00000368838.1:c.1045G>T	ENSP00000357831.1:p.Val349Phe
ENST00000368841.6:c.*995G>T	ENSP00000357834.2:n.*995G>T
ENST00000368843.7:c.1324G>T	ENSP00000357836.3:p.Val442Phe
ENST00000458013.6:c.1324G>T	ENSP00000400333.2:p.Val442Phe
NM_030918.5:c.1324G>T	NP_112180.4:p.Val442Phe
XM_005245509.1:c.1324G>T	XP_005245566.1:p.Val442Phe
XM_005245510.2:c.1015G>T	XP_005245567.1:p.Val339Phe
XM_005245511.3:c.766G>T	XP_005245568.1:p.Val256Phe
XM_011510024.1:c.1021G>T	XP_011508326.1:p.Val341Phe
XM_011510025.1:c.961G>T	XP_011508327.1:p.Val321Phe
NM_001330723.1:c.1324G>T	NP_001317652.1:p.Val442Phe
XM_005245510.3:c.1015G>T	XP_005245567.1:p.Val339Phe
XM_005245511.4:c.766G>T	XP_005245568.1:p.Val256Phe
XM_011510024.2:c.1021G>T	XP_011508326.1:p.Val341Phe
XM_011510025.2:c.961G>T	XP_011508327.1:p.Val321Phe
XM_017002417.1:c.961G>T	XP_016857906.1:p.Val321Phe
XM_024450038.1:c.766G>T	XP_024305806.1:p.Val256Phe
XM_024450039.1:c.766G>T	XP_024305807.1:p.Val256Phe
NM_001330723.2:c.1324G>T MANE Select	NP_001317652.1:p.Val442Phe
NM_030918.6:c.1324G>T	NP_112180.4:p.Val442Phe