Canonical Allele Identifier: CA341972203

Gene: SNX27

Linked Data

• MyVariant Identifiers: chr1:g.151664996T>C (hg19) ; chr1:g.151692520T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151692520T>C , CM000663.2:g.151692520T>C	GRCh38
NC_000001.10:g.151664996T>C , CM000663.1:g.151664996T>C	GRCh37
NC_000001.9:g.149931620T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000368838.2:c.922T>C
ENST00000368841.7:c.*996T>C	ENSP00000357834.2:n.*996T>C
ENST00000368843.8:c.1325T>C	ENSP00000357836.3:p.Val442Ala
ENST00000458013.7:c.1325T>C MANE Select	ENSP00000400333.2:p.Val442Ala
ENST00000642349.1:c.1059T>C	ENSP00000494331.1:n.1059T>C
ENST00000642376.1:c.962T>C	ENSP00000496645.1:p.Val321Ala
ENST00000642479.1:c.*703T>C	ENSP00000496775.1:n.*703T>C
ENST00000643179.1:n.1133T>C
ENST00000643937.1:n.1003T>C
ENST00000644970.1:n.1323T>C
ENST00000647328.1:n.1046T>C
ENST00000647551.1:n.4774T>C
ENST00000368838.1:c.1046T>C	ENSP00000357831.1:p.Val349Ala
ENST00000368841.6:c.*996T>C	ENSP00000357834.2:n.*996T>C
ENST00000368843.7:c.1325T>C	ENSP00000357836.3:p.Val442Ala
ENST00000458013.6:c.1325T>C	ENSP00000400333.2:p.Val442Ala
NM_030918.5:c.1325T>C	NP_112180.4:p.Val442Ala
XM_005245509.1:c.1325T>C	XP_005245566.1:p.Val442Ala
XM_005245510.2:c.1016T>C	XP_005245567.1:p.Val339Ala
XM_005245511.3:c.767T>C	XP_005245568.1:p.Val256Ala
XM_011510024.1:c.1022T>C	XP_011508326.1:p.Val341Ala
XM_011510025.1:c.962T>C	XP_011508327.1:p.Val321Ala
NM_001330723.1:c.1325T>C	NP_001317652.1:p.Val442Ala
XM_005245510.3:c.1016T>C	XP_005245567.1:p.Val339Ala
XM_005245511.4:c.767T>C	XP_005245568.1:p.Val256Ala
XM_011510024.2:c.1022T>C	XP_011508326.1:p.Val341Ala
XM_011510025.2:c.962T>C	XP_011508327.1:p.Val321Ala
XM_017002417.1:c.962T>C	XP_016857906.1:p.Val321Ala
XM_024450038.1:c.767T>C	XP_024305806.1:p.Val256Ala
XM_024450039.1:c.767T>C	XP_024305807.1:p.Val256Ala
NM_001330723.2:c.1325T>C MANE Select	NP_001317652.1:p.Val442Ala
NM_030918.6:c.1325T>C	NP_112180.4:p.Val442Ala