Canonical Allele Identifier: CA346210066

Gene: SNX17

Linked Data

• MyVariant Identifiers: chr2:g.27598404A>C (hg19) ; chr2:g.27375537A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375537A>C , CM000664.2:g.27375537A>C	GRCh38
NC_000002.11:g.27598404A>C , CM000664.1:g.27598404A>C	GRCh37
NC_000002.10:g.27451908A>C	NCBI36
NG_028219.1:g.10208T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.806A>C MANE Select	ENSP00000233575.2:p.Tyr269Ser
ENST00000233575.6:c.806A>C	ENSP00000233575.2:p.Tyr269Ser
ENST00000427123.5:c.*616A>C	ENSP00000405399.1:n.*616A>C
ENST00000440760.5:c.*651A>C	ENSP00000399727.1:n.*651A>C
ENST00000453453.1:c.*333A>C	ENSP00000401922.1:n.*333A>C
ENST00000493711.1:n.523A>C
ENST00000537606.5:c.731A>C	ENSP00000439208.1:p.Tyr244Ser
NM_001267059.1:c.770A>C	NP_001253988.1:p.Tyr257Ser
NM_001267060.1:c.731A>C	NP_001253989.1:p.Tyr244Ser
NM_001267061.1:c.746A>C	NP_001253990.1:p.Tyr249Ser
NM_014748.3:c.806A>C	NP_055563.1:p.Tyr269Ser
NR_049782.1:n.1179A>C
NR_049783.1:n.1152A>C
NR_049784.1:n.1128A>C
NR_049785.1:n.1061A>C
NR_049786.1:n.1010A>C
NR_049787.1:n.861A>C
NR_049788.1:n.791A>C
XM_011533203.1:c.164A>C	XP_011531505.1:p.Tyr55Ser
XM_011533203.2:c.164A>C	XP_011531505.1:p.Tyr55Ser
XM_017005405.2:c.164A>C	XP_016860894.1:p.Tyr55Ser
NM_014748.4:c.806A>C MANE Select	NP_055563.1:p.Tyr269Ser
NM_001267059.2:c.770A>C	NP_001253988.1:p.Tyr257Ser
NM_001267061.2:c.746A>C	NP_001253990.1:p.Tyr249Ser
NR_049782.2:n.1059A>C
NR_049783.2:n.1032A>C
NR_049784.2:n.1008A>C
NR_049785.2:n.941A>C
NR_049786.2:n.890A>C
NR_049787.2:n.741A>C
NR_049788.2:n.671A>C
NM_001267060.2:c.731A>C	NP_001253989.1:p.Tyr244Ser