Canonical Allele Identifier: CA346210060

Gene: SNX17

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.805T>A MANE Select	ENSP00000233575.2:p.Tyr269Asn
ENST00000233575.6:c.805T>A	ENSP00000233575.2:p.Tyr269Asn
ENST00000427123.5:c.*615T>A	ENSP00000405399.1:n.*615T>A
ENST00000440760.5:c.*650T>A	ENSP00000399727.1:n.*650T>A
ENST00000453453.1:c.*332T>A	ENSP00000401922.1:n.*332T>A
ENST00000493711.1:n.522T>A
ENST00000537606.5:c.730T>A	ENSP00000439208.1:p.Tyr244Asn
NM_001267059.1:c.769T>A	NP_001253988.1:p.Tyr257Asn
NM_001267060.1:c.730T>A	NP_001253989.1:p.Tyr244Asn
NM_001267061.1:c.745T>A	NP_001253990.1:p.Tyr249Asn
NM_014748.3:c.805T>A	NP_055563.1:p.Tyr269Asn
NR_049782.1:n.1178T>A
NR_049783.1:n.1151T>A
NR_049784.1:n.1127T>A
NR_049785.1:n.1060T>A
NR_049786.1:n.1009T>A
NR_049787.1:n.860T>A
NR_049788.1:n.790T>A
XM_011533203.1:c.163T>A	XP_011531505.1:p.Tyr55Asn
XM_011533203.2:c.163T>A	XP_011531505.1:p.Tyr55Asn
XM_017005405.2:c.163T>A	XP_016860894.1:p.Tyr55Asn
NM_014748.4:c.805T>A MANE Select	NP_055563.1:p.Tyr269Asn
NM_001267059.2:c.769T>A	NP_001253988.1:p.Tyr257Asn
NM_001267061.2:c.745T>A	NP_001253990.1:p.Tyr249Asn
NR_049782.2:n.1058T>A
NR_049783.2:n.1031T>A
NR_049784.2:n.1007T>A
NR_049785.2:n.940T>A
NR_049786.2:n.889T>A
NR_049787.2:n.740T>A
NR_049788.2:n.670T>A
NM_001267060.2:c.730T>A	NP_001253989.1:p.Tyr244Asn