Canonical Allele Identifier: CA1577572

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27376169G>A , CM000664.2:g.27376169G>A	GRCh38
NC_000002.11:g.27599036G>A , CM000664.1:g.27599036G>A	GRCh37
NC_000002.10:g.27452540G>A	NCBI36
NG_028219.1:g.9576C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_014748.4:c.1168G>A MANE Select	NP_055563.1:p.Gly390Ser
ENST00000233575.7:c.1168G>A MANE Select	ENSP00000233575.2:p.Gly390Ser
NM_001267059.1:c.1132G>A	NP_001253988.1:p.Gly378Ser
NM_001267059.2:c.1132G>A	NP_001253988.1:p.Gly378Ser
NM_001267060.1:c.1093G>A	NP_001253989.1:p.Gly365Ser
NM_001267060.2:c.1093G>A	NP_001253989.1:p.Gly365Ser
NM_001267061.1:c.1108G>A	NP_001253990.1:p.Gly370Ser
NM_001267061.2:c.1108G>A	NP_001253990.1:p.Gly370Ser
NM_014748.3:c.1168G>A	NP_055563.1:p.Gly390Ser
NR_049782.1:n.1541G>A
NR_049782.2:n.1421G>A
NR_049783.1:n.1514G>A
NR_049783.2:n.1394G>A
NR_049784.1:n.1490G>A
NR_049784.2:n.1370G>A
NR_049785.1:n.1423G>A
NR_049785.2:n.1303G>A
NR_049786.1:n.1372G>A
NR_049786.2:n.1252G>A
NR_049787.1:n.1223G>A
NR_049787.2:n.1103G>A
NR_049788.1:n.1153G>A
NR_049788.2:n.1033G>A
ENST00000233575.6:c.1168G>A	ENSP00000233575.2:p.Gly390Ser
ENST00000427123.5:c.*978G>A	ENSP00000405399.1:n.*978G>A
ENST00000440760.5:c.*1013G>A	ENSP00000399727.1:n.*1013G>A
ENST00000453453.1:c.*695G>A	ENSP00000401922.1:n.*695G>A
ENST00000537606.5:c.1093G>A	ENSP00000439208.1:p.Gly365Ser
XM_011533203.1:c.526G>A	XP_011531505.1:p.Gly176Ser
XM_011533203.2:c.526G>A	XP_011531505.1:p.Gly176Ser
XM_017005405.2:c.526G>A	XP_016860894.1:p.Gly176Ser