Canonical Allele Identifier: CA1240248053

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375144C= , CM000664.2:g.27375144C=	GRCh38
NC_000002.11:g.27598011C= , CM000664.1:g.27598011C=	GRCh37
NC_000002.10:g.27451515C=	NCBI36
NG_009305.1:g.314G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.765C= MANE Select	ENSP00000233575.2:p.Ser255=
ENST00000233575.6:c.765C=	ENSP00000233575.2:p.Ser255=
ENST00000427123.5:c.*575C=	ENSP00000405399.1:n.*575C=
ENST00000440760.5:c.*610C=	ENSP00000399727.1:n.*610C=
ENST00000453453.1:c.*292C=	ENSP00000401922.1:n.*292C=
ENST00000493711.1:n.482C=
ENST00000494893.5:n.941C=
ENST00000537606.5:c.690C=	ENSP00000439208.1:p.Ser230=
NM_001267059.1:c.729C=	NP_001253988.1:p.Ser243=
NM_001267060.1:c.690C=	NP_001253989.1:p.Ser230=
NM_001267061.1:c.705C=	NP_001253990.1:p.Ser235=
NM_014748.3:c.765C=	NP_055563.1:p.Ser255=
NR_049782.1:n.1138C=
NR_049783.1:n.1111C=
NR_049784.1:n.1087C=
NR_049785.1:n.1020C=
NR_049786.1:n.969C=
NR_049787.1:n.820C=
NR_049788.1:n.750C=
XM_011533203.1:c.123C=	XP_011531505.1:p.Ser41=
XM_011533203.2:c.123C=	XP_011531505.1:p.Ser41=
XM_017005405.2:c.123C=	XP_016860894.1:p.Ser41=
NM_014748.4:c.765C= MANE Select	NP_055563.1:p.Ser255=
NM_001267059.2:c.729C=	NP_001253988.1:p.Ser243=
NM_001267061.2:c.705C=	NP_001253990.1:p.Ser235=
NR_049782.2:n.1018C=
NR_049783.2:n.991C=
NR_049784.2:n.967C=
NR_049785.2:n.900C=
NR_049786.2:n.849C=
NR_049787.2:n.700C=
NR_049788.2:n.630C=
NM_001267060.2:c.690C=	NP_001253989.1:p.Ser230=