Canonical Allele Identifier: CA1240248044

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375125C= , CM000664.2:g.27375125C=	GRCh38
NC_000002.11:g.27597992C= , CM000664.1:g.27597992C=	GRCh37
NC_000002.10:g.27451496C=	NCBI36
NG_009305.1:g.333G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.746C= MANE Select	ENSP00000233575.2:p.Ser249=
ENST00000233575.6:c.746C=	ENSP00000233575.2:p.Ser249=
ENST00000427123.5:c.*556C=	ENSP00000405399.1:n.*556C=
ENST00000440760.5:c.*591C=	ENSP00000399727.1:n.*591C=
ENST00000453453.1:c.*273C=	ENSP00000401922.1:n.*273C=
ENST00000493711.1:n.463C=
ENST00000494893.5:n.922C=
ENST00000537606.5:c.671C=	ENSP00000439208.1:p.Ser224=
NM_001267059.1:c.710C=	NP_001253988.1:p.Ser237=
NM_001267060.1:c.671C=	NP_001253989.1:p.Ser224=
NM_001267061.1:c.686C=	NP_001253990.1:p.Ser229=
NM_014748.3:c.746C=	NP_055563.1:p.Ser249=
NR_049782.1:n.1119C=
NR_049783.1:n.1092C=
NR_049784.1:n.1068C=
NR_049785.1:n.1001C=
NR_049786.1:n.950C=
NR_049787.1:n.801C=
NR_049788.1:n.731C=
XM_011533203.1:c.104C=	XP_011531505.1:p.Ser35=
XM_011533203.2:c.104C=	XP_011531505.1:p.Ser35=
XM_017005405.2:c.104C=	XP_016860894.1:p.Ser35=
NM_014748.4:c.746C= MANE Select	NP_055563.1:p.Ser249=
NM_001267059.2:c.710C=	NP_001253988.1:p.Ser237=
NM_001267061.2:c.686C=	NP_001253990.1:p.Ser229=
NR_049782.2:n.999C=
NR_049783.2:n.972C=
NR_049784.2:n.948C=
NR_049785.2:n.881C=
NR_049786.2:n.830C=
NR_049787.2:n.681C=
NR_049788.2:n.611C=
NM_001267060.2:c.671C=	NP_001253989.1:p.Ser224=