Canonical Allele Identifier: CA346210062

Gene: SNX17

Linked Data

• MyVariant Identifiers: chr2:g.27598403T>G (hg19) ; chr2:g.27375536T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375536T>G , CM000664.2:g.27375536T>G	GRCh38
NC_000002.11:g.27598403T>G , CM000664.1:g.27598403T>G	GRCh37
NC_000002.10:g.27451907T>G	NCBI36
NG_028219.1:g.10209A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.805T>G MANE Select	ENSP00000233575.2:p.Tyr269Asp
ENST00000233575.6:c.805T>G	ENSP00000233575.2:p.Tyr269Asp
ENST00000427123.5:c.*615T>G	ENSP00000405399.1:n.*615T>G
ENST00000440760.5:c.*650T>G	ENSP00000399727.1:n.*650T>G
ENST00000453453.1:c.*332T>G	ENSP00000401922.1:n.*332T>G
ENST00000493711.1:n.522T>G
ENST00000537606.5:c.730T>G	ENSP00000439208.1:p.Tyr244Asp
NM_001267059.1:c.769T>G	NP_001253988.1:p.Tyr257Asp
NM_001267060.1:c.730T>G	NP_001253989.1:p.Tyr244Asp
NM_001267061.1:c.745T>G	NP_001253990.1:p.Tyr249Asp
NM_014748.3:c.805T>G	NP_055563.1:p.Tyr269Asp
NR_049782.1:n.1178T>G
NR_049783.1:n.1151T>G
NR_049784.1:n.1127T>G
NR_049785.1:n.1060T>G
NR_049786.1:n.1009T>G
NR_049787.1:n.860T>G
NR_049788.1:n.790T>G
XM_011533203.1:c.163T>G	XP_011531505.1:p.Tyr55Asp
XM_011533203.2:c.163T>G	XP_011531505.1:p.Tyr55Asp
XM_017005405.2:c.163T>G	XP_016860894.1:p.Tyr55Asp
NM_014748.4:c.805T>G MANE Select	NP_055563.1:p.Tyr269Asp
NM_001267059.2:c.769T>G	NP_001253988.1:p.Tyr257Asp
NM_001267061.2:c.745T>G	NP_001253990.1:p.Tyr249Asp
NR_049782.2:n.1058T>G
NR_049783.2:n.1031T>G
NR_049784.2:n.1007T>G
NR_049785.2:n.940T>G
NR_049786.2:n.889T>G
NR_049787.2:n.740T>G
NR_049788.2:n.670T>G
NM_001267060.2:c.730T>G	NP_001253989.1:p.Tyr244Asp