Canonical Allele Identifier: CA341974294

Gene: SNX27

Linked Data

• MyVariant Identifiers: chr1:g.151584883G>C (hg19) ; chr1:g.151612407G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151612407G>C , CM000663.2:g.151612407G>C	GRCh38
NC_000001.10:g.151584883G>C , CM000663.1:g.151584883G>C	GRCh37
NC_000001.9:g.149851507G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368841.7:c.180+26G>C	ENSP00000357834.2:n.180+26G>C
ENST00000368843.8:c.206G>C	ENSP00000357836.3:p.Ser69Thr
ENST00000458013.7:c.206G>C MANE Select	ENSP00000400333.2:p.Ser69Thr
ENST00000642349.1:c.45+26G>C	ENSP00000494331.1:n.45+26G>C
ENST00000642376.1:c.180+26G>C	ENSP00000496645.1:n.180+26G>C
ENST00000642479.1:c.206G>C	ENSP00000496775.1:p.Ser69Thr
ENST00000643179.1:n.14G>C
ENST00000368841.6:c.180+26G>C	ENSP00000357834.2:n.180+26G>C
ENST00000368843.7:c.206G>C	ENSP00000357836.3:p.Ser69Thr
ENST00000458013.6:c.206G>C	ENSP00000400333.2:p.Ser69Thr
NM_030918.5:c.206G>C	NP_112180.4:p.Ser69Thr
XM_005245509.1:c.206G>C	XP_005245566.1:p.Ser69Thr
XM_005245510.2:c.-33G>C	XP_005245567.1:n.-33G>C
XM_005245511.3:c.-248+26G>C	XP_005245568.1:n.-248+26G>C
XM_011510024.1:c.206G>C	XP_011508326.1:p.Ser69Thr
XM_011510025.1:c.180+26G>C	XP_011508327.1:n.180+26G>C
XM_011510026.1:c.206G>C	XP_011508328.1:p.Ser69Thr
NM_001330723.1:c.206G>C	NP_001317652.1:p.Ser69Thr
XM_005245510.3:c.-33G>C	XP_005245567.1:n.-33G>C
XM_005245511.4:c.-248+26G>C	XP_005245568.1:n.-248+26G>C
XM_011510024.2:c.206G>C	XP_011508326.1:p.Ser69Thr
XM_011510025.2:c.180+26G>C	XP_011508327.1:n.180+26G>C
XM_011510026.2:c.206G>C	XP_011508328.1:p.Ser69Thr
XM_017002417.1:c.180+26G>C	XP_016857906.1:n.180+26G>C
XM_024450038.1:c.-121G>C	XP_024305806.1:n.-121G>C
XM_024450039.1:c.-121G>C	XP_024305807.1:n.-121G>C
NM_001330723.2:c.206G>C MANE Select	NP_001317652.1:p.Ser69Thr
NM_030918.6:c.206G>C	NP_112180.4:p.Ser69Thr