Canonical Allele Identifier: CA1240248788

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375546T= , CM000664.2:g.27375546T=	GRCh38
NC_000002.11:g.27598413T= , CM000664.1:g.27598413T=	GRCh37
NC_000002.10:g.27451917T=	NCBI36
NG_028219.1:g.10199A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.815T= MANE Select	ENSP00000233575.2:p.Leu272=
ENST00000233575.6:c.815T=	ENSP00000233575.2:p.Leu272=
ENST00000427123.5:c.*625T=	ENSP00000405399.1:n.*625T=
ENST00000440760.5:c.*660T=	ENSP00000399727.1:n.*660T=
ENST00000453453.1:c.*342T=	ENSP00000401922.1:n.*342T=
ENST00000493711.1:n.532T=
ENST00000537606.5:c.740T=	ENSP00000439208.1:p.Leu247=
NM_001267059.1:c.779T=	NP_001253988.1:p.Leu260=
NM_001267060.1:c.740T=	NP_001253989.1:p.Leu247=
NM_001267061.1:c.755T=	NP_001253990.1:p.Leu252=
NM_014748.3:c.815T=	NP_055563.1:p.Leu272=
NR_049782.1:n.1188T=
NR_049783.1:n.1161T=
NR_049784.1:n.1137T=
NR_049785.1:n.1070T=
NR_049786.1:n.1019T=
NR_049787.1:n.870T=
NR_049788.1:n.800T=
XM_011533203.1:c.173T=	XP_011531505.1:p.Leu58=
XM_011533203.2:c.173T=	XP_011531505.1:p.Leu58=
XM_017005405.2:c.173T=	XP_016860894.1:p.Leu58=
NM_014748.4:c.815T= MANE Select	NP_055563.1:p.Leu272=
NM_001267059.2:c.779T=	NP_001253988.1:p.Leu260=
NM_001267061.2:c.755T=	NP_001253990.1:p.Leu252=
NR_049782.2:n.1068T=
NR_049783.2:n.1041T=
NR_049784.2:n.1017T=
NR_049785.2:n.950T=
NR_049786.2:n.899T=
NR_049787.2:n.750T=
NR_049788.2:n.680T=
NM_001267060.2:c.740T=	NP_001253989.1:p.Leu247=