Canonical Allele Identifier: CA1240248768

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375540G= , CM000664.2:g.27375540G=	GRCh38
NC_000002.11:g.27598407G= , CM000664.1:g.27598407G=	GRCh37
NC_000002.10:g.27451911G=	NCBI36
NG_028219.1:g.10205C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.809G= MANE Select	ENSP00000233575.2:p.Gly270=
ENST00000233575.6:c.809G=	ENSP00000233575.2:p.Gly270=
ENST00000427123.5:c.*619G=	ENSP00000405399.1:n.*619G=
ENST00000440760.5:c.*654G=	ENSP00000399727.1:n.*654G=
ENST00000453453.1:c.*336G=	ENSP00000401922.1:n.*336G=
ENST00000493711.1:n.526G=
ENST00000537606.5:c.734G=	ENSP00000439208.1:p.Gly245=
NM_001267059.1:c.773G=	NP_001253988.1:p.Gly258=
NM_001267060.1:c.734G=	NP_001253989.1:p.Gly245=
NM_001267061.1:c.749G=	NP_001253990.1:p.Gly250=
NM_014748.3:c.809G=	NP_055563.1:p.Gly270=
NR_049782.1:n.1182G=
NR_049783.1:n.1155G=
NR_049784.1:n.1131G=
NR_049785.1:n.1064G=
NR_049786.1:n.1013G=
NR_049787.1:n.864G=
NR_049788.1:n.794G=
XM_011533203.1:c.167G=	XP_011531505.1:p.Gly56=
XM_011533203.2:c.167G=	XP_011531505.1:p.Gly56=
XM_017005405.2:c.167G=	XP_016860894.1:p.Gly56=
NM_014748.4:c.809G= MANE Select	NP_055563.1:p.Gly270=
NM_001267059.2:c.773G=	NP_001253988.1:p.Gly258=
NM_001267061.2:c.749G=	NP_001253990.1:p.Gly250=
NR_049782.2:n.1062G=
NR_049783.2:n.1035G=
NR_049784.2:n.1011G=
NR_049785.2:n.944G=
NR_049786.2:n.893G=
NR_049787.2:n.744G=
NR_049788.2:n.674G=
NM_001267060.2:c.734G=	NP_001253989.1:p.Gly245=