Canonical Allele Identifier: CA420748174

Gene: SNX27

Linked Data

• gnomAD v4: 1-151612372-G-A
• MyVariant Identifiers: chr1:g.151584848G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151612372G>A , CM000663.2:g.151612372G>A	GRCh38
NC_000001.10:g.151584848G>A , CM000663.1:g.151584848G>A	GRCh37
NC_000001.9:g.149851472G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368841.7:c.171G>A	ENSP00000357834.2:p.Val57=
ENST00000368843.8:c.171G>A	ENSP00000357836.3:p.Val57=
ENST00000458013.7:c.171G>A MANE Select	ENSP00000400333.2:p.Val57=
ENST00000642349.1:c.36G>A	ENSP00000494331.1:p.Val12=
ENST00000642376.1:c.171G>A	ENSP00000496645.1:p.Val57=
ENST00000642479.1:c.171G>A	ENSP00000496775.1:p.Val57=
ENST00000368841.6:c.171G>A	ENSP00000357834.2:p.Val57=
ENST00000368843.7:c.171G>A	ENSP00000357836.3:p.Val57=
ENST00000458013.6:c.171G>A	ENSP00000400333.2:p.Val57=
NM_030918.5:c.171G>A	NP_112180.4:p.Val57=
XM_005245509.1:c.171G>A	XP_005245566.1:p.Val57=
XM_005245511.3:c.-257G>A	XP_005245568.1:n.-257G>A
XM_011510024.1:c.171G>A	XP_011508326.1:p.Val57=
XM_011510025.1:c.171G>A	XP_011508327.1:p.Val57=
XM_011510026.1:c.171G>A	XP_011508328.1:p.Val57=
NM_001330723.1:c.171G>A	NP_001317652.1:p.Val57=
XM_005245511.4:c.-257G>A	XP_005245568.1:n.-257G>A
XM_011510024.2:c.171G>A	XP_011508326.1:p.Val57=
XM_011510025.2:c.171G>A	XP_011508327.1:p.Val57=
XM_011510026.2:c.171G>A	XP_011508328.1:p.Val57=
XM_017002417.1:c.171G>A	XP_016857906.1:p.Val57=
XM_024450038.1:c.-156G>A	XP_024305806.1:n.-156G>A
XM_024450039.1:c.-156G>A	XP_024305807.1:n.-156G>A
NM_001330723.2:c.171G>A MANE Select	NP_001317652.1:p.Val57=
NM_030918.6:c.171G>A	NP_112180.4:p.Val57=