Canonical Allele Identifier: CA1240249445

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375064G= , CM000664.2:g.27375064G=	GRCh38
NC_000002.11:g.27597931G= , CM000664.1:g.27597931G=	GRCh37
NC_000002.10:g.27451435G=	NCBI36
NG_009305.1:g.394C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.685G= MANE Select	ENSP00000233575.2:p.Val229=
ENST00000233575.6:c.685G=	ENSP00000233575.2:p.Val229=
ENST00000427123.5:c.*495G=	ENSP00000405399.1:n.*495G=
ENST00000440760.5:c.*530G=	ENSP00000399727.1:n.*530G=
ENST00000453453.1:c.*212G=	ENSP00000401922.1:n.*212G=
ENST00000493711.1:n.402G=
ENST00000494893.5:n.861G=
ENST00000537606.5:c.610G=	ENSP00000439208.1:p.Val204=
NM_001267059.1:c.649G=	NP_001253988.1:p.Val217=
NM_001267060.1:c.610G=	NP_001253989.1:p.Val204=
NM_001267061.1:c.625G=	NP_001253990.1:p.Val209=
NM_014748.3:c.685G=	NP_055563.1:p.Val229=
NR_049782.1:n.1058G=
NR_049783.1:n.1031G=
NR_049784.1:n.1007G=
NR_049785.1:n.940G=
NR_049786.1:n.889G=
NR_049787.1:n.740G=
NR_049788.1:n.670G=
XM_011533203.1:c.43G=	XP_011531505.1:p.Val15=
XM_011533203.2:c.43G=	XP_011531505.1:p.Val15=
XM_017005405.2:c.43G=	XP_016860894.1:p.Val15=
NM_014748.4:c.685G= MANE Select	NP_055563.1:p.Val229=
NM_001267059.2:c.649G=	NP_001253988.1:p.Val217=
NM_001267061.2:c.625G=	NP_001253990.1:p.Val209=
NR_049782.2:n.938G=
NR_049783.2:n.911G=
NR_049784.2:n.887G=
NR_049785.2:n.820G=
NR_049786.2:n.769G=
NR_049787.2:n.620G=
NR_049788.2:n.550G=
NM_001267060.2:c.610G=	NP_001253989.1:p.Val204=