Canonical Allele Identifier: CA1240248750

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375535C= , CM000664.2:g.27375535C=	GRCh38
NC_000002.11:g.27598402C= , CM000664.1:g.27598402C=	GRCh37
NC_000002.10:g.27451906C=	NCBI36
NG_028219.1:g.10210G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.804C= MANE Select	ENSP00000233575.2:p.His268=
ENST00000233575.6:c.804C=	ENSP00000233575.2:p.His268=
ENST00000427123.5:c.*614C=	ENSP00000405399.1:n.*614C=
ENST00000440760.5:c.*649C=	ENSP00000399727.1:n.*649C=
ENST00000453453.1:c.*331C=	ENSP00000401922.1:n.*331C=
ENST00000493711.1:n.521C=
ENST00000537606.5:c.729C=	ENSP00000439208.1:p.His243=
NM_001267059.1:c.768C=	NP_001253988.1:p.His256=
NM_001267060.1:c.729C=	NP_001253989.1:p.His243=
NM_001267061.1:c.744C=	NP_001253990.1:p.His248=
NM_014748.3:c.804C=	NP_055563.1:p.His268=
NR_049782.1:n.1177C=
NR_049783.1:n.1150C=
NR_049784.1:n.1126C=
NR_049785.1:n.1059C=
NR_049786.1:n.1008C=
NR_049787.1:n.859C=
NR_049788.1:n.789C=
XM_011533203.1:c.162C=	XP_011531505.1:p.His54=
XM_011533203.2:c.162C=	XP_011531505.1:p.His54=
XM_017005405.2:c.162C=	XP_016860894.1:p.His54=
NM_014748.4:c.804C= MANE Select	NP_055563.1:p.His268=
NM_001267059.2:c.768C=	NP_001253988.1:p.His256=
NM_001267061.2:c.744C=	NP_001253990.1:p.His248=
NR_049782.2:n.1057C=
NR_049783.2:n.1030C=
NR_049784.2:n.1006C=
NR_049785.2:n.939C=
NR_049786.2:n.888C=
NR_049787.2:n.739C=
NR_049788.2:n.669C=
NM_001267060.2:c.729C=	NP_001253989.1:p.His243=