Canonical Allele Identifier: CA346210030

Gene: SNX17

Linked Data

• MyVariant Identifiers: chr2:g.27598394C>A (hg19) ; chr2:g.27375527C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375527C>A , CM000664.2:g.27375527C>A	GRCh38
NC_000002.11:g.27598394C>A , CM000664.1:g.27598394C>A	GRCh37
NC_000002.10:g.27451898C>A	NCBI36
NG_028219.1:g.10218G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.796C>A MANE Select	ENSP00000233575.2:p.Leu266Met
ENST00000233575.6:c.796C>A	ENSP00000233575.2:p.Leu266Met
ENST00000427123.5:c.*606C>A	ENSP00000405399.1:n.*606C>A
ENST00000440760.5:c.*641C>A	ENSP00000399727.1:n.*641C>A
ENST00000453453.1:c.*323C>A	ENSP00000401922.1:n.*323C>A
ENST00000493711.1:n.513C>A
ENST00000537606.5:c.721C>A	ENSP00000439208.1:p.Leu241Met
NM_001267059.1:c.760C>A	NP_001253988.1:p.Leu254Met
NM_001267060.1:c.721C>A	NP_001253989.1:p.Leu241Met
NM_001267061.1:c.736C>A	NP_001253990.1:p.Leu246Met
NM_014748.3:c.796C>A	NP_055563.1:p.Leu266Met
NR_049782.1:n.1169C>A
NR_049783.1:n.1142C>A
NR_049784.1:n.1118C>A
NR_049785.1:n.1051C>A
NR_049786.1:n.1000C>A
NR_049787.1:n.851C>A
NR_049788.1:n.781C>A
XM_011533203.1:c.154C>A	XP_011531505.1:p.Leu52Met
XM_011533203.2:c.154C>A	XP_011531505.1:p.Leu52Met
XM_017005405.2:c.154C>A	XP_016860894.1:p.Leu52Met
NM_014748.4:c.796C>A MANE Select	NP_055563.1:p.Leu266Met
NM_001267059.2:c.760C>A	NP_001253988.1:p.Leu254Met
NM_001267061.2:c.736C>A	NP_001253990.1:p.Leu246Met
NR_049782.2:n.1049C>A
NR_049783.2:n.1022C>A
NR_049784.2:n.998C>A
NR_049785.2:n.931C>A
NR_049786.2:n.880C>A
NR_049787.2:n.731C>A
NR_049788.2:n.661C>A
NM_001267060.2:c.721C>A	NP_001253989.1:p.Leu241Met