Canonical Allele Identifier: CA425415840

Gene: SNX17

Linked Data

• MyVariant Identifiers: chr2:g.27598011C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375144C>G , CM000664.2:g.27375144C>G	GRCh38
NC_000002.11:g.27598011C>G , CM000664.1:g.27598011C>G	GRCh37
NC_000002.10:g.27451515C>G	NCBI36
NG_009305.1:g.314G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.765C>G MANE Select	ENSP00000233575.2:p.Ser255=
ENST00000233575.6:c.765C>G	ENSP00000233575.2:p.Ser255=
ENST00000427123.5:c.*575C>G	ENSP00000405399.1:n.*575C>G
ENST00000440760.5:c.*610C>G	ENSP00000399727.1:n.*610C>G
ENST00000453453.1:c.*292C>G	ENSP00000401922.1:n.*292C>G
ENST00000493711.1:n.482C>G
ENST00000494893.5:n.941C>G
ENST00000537606.5:c.690C>G	ENSP00000439208.1:p.Ser230=
NM_001267059.1:c.729C>G	NP_001253988.1:p.Ser243=
NM_001267060.1:c.690C>G	NP_001253989.1:p.Ser230=
NM_001267061.1:c.705C>G	NP_001253990.1:p.Ser235=
NM_014748.3:c.765C>G	NP_055563.1:p.Ser255=
NR_049782.1:n.1138C>G
NR_049783.1:n.1111C>G
NR_049784.1:n.1087C>G
NR_049785.1:n.1020C>G
NR_049786.1:n.969C>G
NR_049787.1:n.820C>G
NR_049788.1:n.750C>G
XM_011533203.1:c.123C>G	XP_011531505.1:p.Ser41=
XM_011533203.2:c.123C>G	XP_011531505.1:p.Ser41=
XM_017005405.2:c.123C>G	XP_016860894.1:p.Ser41=
NM_014748.4:c.765C>G MANE Select	NP_055563.1:p.Ser255=
NM_001267059.2:c.729C>G	NP_001253988.1:p.Ser243=
NM_001267061.2:c.705C>G	NP_001253990.1:p.Ser235=
NR_049782.2:n.1018C>G
NR_049783.2:n.991C>G
NR_049784.2:n.967C>G
NR_049785.2:n.900C>G
NR_049786.2:n.849C>G
NR_049787.2:n.700C>G
NR_049788.2:n.630C>G
NM_001267060.2:c.690C>G	NP_001253989.1:p.Ser230=