Canonical Allele Identifier: CA2581758095

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375054A>C , CM000664.2:g.27375054A>C	GRCh38
NC_000002.11:g.27597921A>C , CM000664.1:g.27597921A>C	GRCh37
NC_000002.10:g.27451425A>C	NCBI36
NG_009305.1:g.404T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.682-7A>C MANE Select	ENSP00000233575.2:n.682-7A>C
ENST00000233575.6:c.682-7A>C	ENSP00000233575.2:n.682-7A>C
ENST00000427123.5:c.*492-7A>C	ENSP00000405399.1:n.*492-7A>C
ENST00000440760.5:c.*527-7A>C	ENSP00000399727.1:n.*527-7A>C
ENST00000453453.1:c.*209-7A>C	ENSP00000401922.1:n.*209-7A>C
ENST00000493711.1:n.392A>C
ENST00000494893.5:n.858-7A>C
ENST00000537606.5:c.607-7A>C	ENSP00000439208.1:n.607-7A>C
NM_001267059.1:c.646-7A>C	NP_001253988.1:n.646-7A>C
NM_001267060.1:c.607-7A>C	NP_001253989.1:n.607-7A>C
NM_001267061.1:c.622-7A>C	NP_001253990.1:n.622-7A>C
NM_014748.3:c.682-7A>C	NP_055563.1:n.682-7A>C
NR_049782.1:n.1055-7A>C
NR_049783.1:n.1028-7A>C
NR_049784.1:n.1004-7A>C
NR_049785.1:n.937-7A>C
NR_049786.1:n.886-7A>C
NR_049787.1:n.737-7A>C
NR_049788.1:n.667-7A>C
XM_011533203.1:c.40-7A>C	XP_011531505.1:n.40-7A>C
XM_011533203.2:c.40-7A>C	XP_011531505.1:n.40-7A>C
XM_017005405.2:c.40-7A>C	XP_016860894.1:n.40-7A>C
NM_014748.4:c.682-7A>C MANE Select	NP_055563.1:n.682-7A>C
NM_001267059.2:c.646-7A>C	NP_001253988.1:n.646-7A>C
NM_001267061.2:c.622-7A>C	NP_001253990.1:n.622-7A>C
NR_049782.2:n.935-7A>C
NR_049783.2:n.908-7A>C
NR_049784.2:n.884-7A>C
NR_049785.2:n.817-7A>C
NR_049786.2:n.766-7A>C
NR_049787.2:n.617-7A>C
NR_049788.2:n.547-7A>C
NM_001267060.2:c.607-7A>C	NP_001253989.1:n.607-7A>C