Canonical Allele Identifier: CA425415747

Gene: SNX17

Linked Data

• MyVariant Identifiers: chr2:g.27597951G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375084G>C , CM000664.2:g.27375084G>C	GRCh38
NC_000002.11:g.27597951G>C , CM000664.1:g.27597951G>C	GRCh37
NC_000002.10:g.27451455G>C	NCBI36
NG_009305.1:g.374C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.705G>C MANE Select	ENSP00000233575.2:p.Gly235=
ENST00000233575.6:c.705G>C	ENSP00000233575.2:p.Gly235=
ENST00000427123.5:c.*515G>C	ENSP00000405399.1:n.*515G>C
ENST00000440760.5:c.*550G>C	ENSP00000399727.1:n.*550G>C
ENST00000453453.1:c.*232G>C	ENSP00000401922.1:n.*232G>C
ENST00000493711.1:n.422G>C
ENST00000494893.5:n.881G>C
ENST00000537606.5:c.630G>C	ENSP00000439208.1:p.Gly210=
NM_001267059.1:c.669G>C	NP_001253988.1:p.Gly223=
NM_001267060.1:c.630G>C	NP_001253989.1:p.Gly210=
NM_001267061.1:c.645G>C	NP_001253990.1:p.Gly215=
NM_014748.3:c.705G>C	NP_055563.1:p.Gly235=
NR_049782.1:n.1078G>C
NR_049783.1:n.1051G>C
NR_049784.1:n.1027G>C
NR_049785.1:n.960G>C
NR_049786.1:n.909G>C
NR_049787.1:n.760G>C
NR_049788.1:n.690G>C
XM_011533203.1:c.63G>C	XP_011531505.1:p.Gly21=
XM_011533203.2:c.63G>C	XP_011531505.1:p.Gly21=
XM_017005405.2:c.63G>C	XP_016860894.1:p.Gly21=
NM_014748.4:c.705G>C MANE Select	NP_055563.1:p.Gly235=
NM_001267059.2:c.669G>C	NP_001253988.1:p.Gly223=
NM_001267061.2:c.645G>C	NP_001253990.1:p.Gly215=
NR_049782.2:n.958G>C
NR_049783.2:n.931G>C
NR_049784.2:n.907G>C
NR_049785.2:n.840G>C
NR_049786.2:n.789G>C
NR_049787.2:n.640G>C
NR_049788.2:n.570G>C
NM_001267060.2:c.630G>C	NP_001253989.1:p.Gly210=