Canonical Allele Identifier: CA346210055

Gene: SNX17

Linked Data

• MyVariant Identifiers: chr2:g.27598402C>A (hg19) ; chr2:g.27375535C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375535C>A , CM000664.2:g.27375535C>A	GRCh38
NC_000002.11:g.27598402C>A , CM000664.1:g.27598402C>A	GRCh37
NC_000002.10:g.27451906C>A	NCBI36
NG_028219.1:g.10210G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.804C>A MANE Select	ENSP00000233575.2:p.His268Gln
ENST00000233575.6:c.804C>A	ENSP00000233575.2:p.His268Gln
ENST00000427123.5:c.*614C>A	ENSP00000405399.1:n.*614C>A
ENST00000440760.5:c.*649C>A	ENSP00000399727.1:n.*649C>A
ENST00000453453.1:c.*331C>A	ENSP00000401922.1:n.*331C>A
ENST00000493711.1:n.521C>A
ENST00000537606.5:c.729C>A	ENSP00000439208.1:p.His243Gln
NM_001267059.1:c.768C>A	NP_001253988.1:p.His256Gln
NM_001267060.1:c.729C>A	NP_001253989.1:p.His243Gln
NM_001267061.1:c.744C>A	NP_001253990.1:p.His248Gln
NM_014748.3:c.804C>A	NP_055563.1:p.His268Gln
NR_049782.1:n.1177C>A
NR_049783.1:n.1150C>A
NR_049784.1:n.1126C>A
NR_049785.1:n.1059C>A
NR_049786.1:n.1008C>A
NR_049787.1:n.859C>A
NR_049788.1:n.789C>A
XM_011533203.1:c.162C>A	XP_011531505.1:p.His54Gln
XM_011533203.2:c.162C>A	XP_011531505.1:p.His54Gln
XM_017005405.2:c.162C>A	XP_016860894.1:p.His54Gln
NM_014748.4:c.804C>A MANE Select	NP_055563.1:p.His268Gln
NM_001267059.2:c.768C>A	NP_001253988.1:p.His256Gln
NM_001267061.2:c.744C>A	NP_001253990.1:p.His248Gln
NR_049782.2:n.1057C>A
NR_049783.2:n.1030C>A
NR_049784.2:n.1006C>A
NR_049785.2:n.939C>A
NR_049786.2:n.888C>A
NR_049787.2:n.739C>A
NR_049788.2:n.669C>A
NM_001267060.2:c.729C>A	NP_001253989.1:p.His243Gln