Canonical Allele Identifier: CA1240248392

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375357C= , CM000664.2:g.27375357C=	GRCh38
NC_000002.11:g.27598224C= , CM000664.1:g.27598224C=	GRCh37
NC_000002.10:g.27451728C=	NCBI36
NG_009305.1:g.101G=
NG_028219.1:g.10388G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.775-149C= MANE Select	ENSP00000233575.2:n.775-149C=
ENST00000233575.6:c.775-149C=	ENSP00000233575.2:n.775-149C=
ENST00000427123.5:c.*585-149C=	ENSP00000405399.1:n.*585-149C=
ENST00000440760.5:c.*620-149C=	ENSP00000399727.1:n.*620-149C=
ENST00000453453.1:c.*302-149C=	ENSP00000401922.1:n.*302-149C=
ENST00000493711.1:n.492-149C=
ENST00000494893.5:n.951-149C=
ENST00000537606.5:c.700-149C=	ENSP00000439208.1:n.700-149C=
NM_001267059.1:c.739-149C=	NP_001253988.1:n.739-149C=
NM_001267060.1:c.700-149C=	NP_001253989.1:n.700-149C=
NM_001267061.1:c.715-149C=	NP_001253990.1:n.715-149C=
NM_014748.3:c.775-149C=	NP_055563.1:n.775-149C=
NR_049782.1:n.1148-149C=
NR_049783.1:n.1121-149C=
NR_049784.1:n.1097-149C=
NR_049785.1:n.1030-149C=
NR_049786.1:n.979-149C=
NR_049787.1:n.830-149C=
NR_049788.1:n.760-149C=
XM_011533203.1:c.133-149C=	XP_011531505.1:n.133-149C=
XM_011533203.2:c.133-149C=	XP_011531505.1:n.133-149C=
XM_017005405.2:c.133-149C=	XP_016860894.1:n.133-149C=
NM_014748.4:c.775-149C= MANE Select	NP_055563.1:n.775-149C=
NM_001267059.2:c.739-149C=	NP_001253988.1:n.739-149C=
NM_001267061.2:c.715-149C=	NP_001253990.1:n.715-149C=
NR_049782.2:n.1028-149C=
NR_049783.2:n.1001-149C=
NR_049784.2:n.977-149C=
NR_049785.2:n.910-149C=
NR_049786.2:n.859-149C=
NR_049787.2:n.710-149C=
NR_049788.2:n.640-149C=
NM_001267060.2:c.700-149C=	NP_001253989.1:n.700-149C=