Canonical Allele Identifier: CA341974084

Gene: SNX27

Linked Data

• gnomAD v4: 1-151612376-G-A
• MyVariant Identifiers: chr1:g.151584852G>A (hg19) ; chr1:g.151612376G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151612376G>A , CM000663.2:g.151612376G>A	GRCh38
NC_000001.10:g.151584852G>A , CM000663.1:g.151584852G>A	GRCh37
NC_000001.9:g.149851476G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368841.7:c.175G>A	ENSP00000357834.2:p.Gly59Ser
ENST00000368843.8:c.175G>A	ENSP00000357836.3:p.Gly59Ser
ENST00000458013.7:c.175G>A MANE Select	ENSP00000400333.2:p.Gly59Ser
ENST00000642349.1:c.40G>A	ENSP00000494331.1:p.Gly14Ser
ENST00000642376.1:c.175G>A	ENSP00000496645.1:p.Gly59Ser
ENST00000642479.1:c.175G>A	ENSP00000496775.1:p.Gly59Ser
ENST00000368841.6:c.175G>A	ENSP00000357834.2:p.Gly59Ser
ENST00000368843.7:c.175G>A	ENSP00000357836.3:p.Gly59Ser
ENST00000458013.6:c.175G>A	ENSP00000400333.2:p.Gly59Ser
NM_030918.5:c.175G>A	NP_112180.4:p.Gly59Ser
XM_005245509.1:c.175G>A	XP_005245566.1:p.Gly59Ser
XM_005245510.2:c.-64G>A	XP_005245567.1:n.-64G>A
XM_005245511.3:c.-253G>A	XP_005245568.1:n.-253G>A
XM_011510024.1:c.175G>A	XP_011508326.1:p.Gly59Ser
XM_011510025.1:c.175G>A	XP_011508327.1:p.Gly59Ser
XM_011510026.1:c.175G>A	XP_011508328.1:p.Gly59Ser
NM_001330723.1:c.175G>A	NP_001317652.1:p.Gly59Ser
XM_005245511.4:c.-253G>A	XP_005245568.1:n.-253G>A
XM_011510024.2:c.175G>A	XP_011508326.1:p.Gly59Ser
XM_011510025.2:c.175G>A	XP_011508327.1:p.Gly59Ser
XM_011510026.2:c.175G>A	XP_011508328.1:p.Gly59Ser
XM_017002417.1:c.175G>A	XP_016857906.1:p.Gly59Ser
XM_024450038.1:c.-152G>A	XP_024305806.1:n.-152G>A
XM_024450039.1:c.-152G>A	XP_024305807.1:n.-152G>A
NM_001330723.2:c.175G>A MANE Select	NP_001317652.1:p.Gly59Ser
NM_030918.6:c.175G>A	NP_112180.4:p.Gly59Ser