Canonical Allele Identifier: CA425415753

Gene: SNX17

Linked Data

• MyVariant Identifiers: chr2:g.27597957C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375090C>A , CM000664.2:g.27375090C>A	GRCh38
NC_000002.11:g.27597957C>A , CM000664.1:g.27597957C>A	GRCh37
NC_000002.10:g.27451461C>A	NCBI36
NG_009305.1:g.368G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.711C>A MANE Select	ENSP00000233575.2:p.Ile237=
ENST00000233575.6:c.711C>A	ENSP00000233575.2:p.Ile237=
ENST00000427123.5:c.*521C>A	ENSP00000405399.1:n.*521C>A
ENST00000440760.5:c.*556C>A	ENSP00000399727.1:n.*556C>A
ENST00000453453.1:c.*238C>A	ENSP00000401922.1:n.*238C>A
ENST00000493711.1:n.428C>A
ENST00000494893.5:n.887C>A
ENST00000537606.5:c.636C>A	ENSP00000439208.1:p.Ile212=
NM_001267059.1:c.675C>A	NP_001253988.1:p.Ile225=
NM_001267060.1:c.636C>A	NP_001253989.1:p.Ile212=
NM_001267061.1:c.651C>A	NP_001253990.1:p.Ile217=
NM_014748.3:c.711C>A	NP_055563.1:p.Ile237=
NR_049782.1:n.1084C>A
NR_049783.1:n.1057C>A
NR_049784.1:n.1033C>A
NR_049785.1:n.966C>A
NR_049786.1:n.915C>A
NR_049787.1:n.766C>A
NR_049788.1:n.696C>A
XM_011533203.1:c.69C>A	XP_011531505.1:p.Ile23=
XM_011533203.2:c.69C>A	XP_011531505.1:p.Ile23=
XM_017005405.2:c.69C>A	XP_016860894.1:p.Ile23=
NM_014748.4:c.711C>A MANE Select	NP_055563.1:p.Ile237=
NM_001267059.2:c.675C>A	NP_001253988.1:p.Ile225=
NM_001267061.2:c.651C>A	NP_001253990.1:p.Ile217=
NR_049782.2:n.964C>A
NR_049783.2:n.937C>A
NR_049784.2:n.913C>A
NR_049785.2:n.846C>A
NR_049786.2:n.795C>A
NR_049787.2:n.646C>A
NR_049788.2:n.576C>A
NM_001267060.2:c.636C>A	NP_001253989.1:p.Ile212=