Canonical Allele Identifier: CA15877765

Gene: SNX29

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.11983775A>G , CM000678.2:g.11983775A>G	GRCh38
NC_000016.9:g.12077632A>G , CM000678.1:g.12077632A>G	GRCh37
NC_000016.8:g.11985133A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000566228.6:c.7+6962A>G MANE Select	ENSP00000456480.1:n.7+6962A>G
ENST00000564111.5:n.69+6962A>G
ENST00000566228.5:c.7+6962A>G	ENSP00000456480.1:n.7+6962A>G
ENST00000569801.5:c.7+6962A>G	ENSP00000457085.1:n.7+6962A>G
NM_032167.4:c.7+6962A>G	NP_115543.3:n.7+6962A>G
XM_005255682.2:c.37+65A>G	XP_005255739.1:n.37+65A>G
XM_005255683.2:c.37+65A>G	XP_005255740.1:n.37+65A>G
XM_011522737.1:c.37+65A>G	XP_011521039.1:n.37+65A>G
XM_011522738.1:c.37+65A>G	XP_011521040.1:n.37+65A>G
XM_011522739.1:c.37+65A>G	XP_011521041.1:n.37+65A>G
XM_011522740.1:c.7+6962A>G	XP_011521042.1:n.7+6962A>G
XM_011522741.1:c.37+65A>G	XP_011521043.1:n.37+65A>G
XM_011522742.1:c.37+65A>G	XP_011521044.1:n.37+65A>G
XM_011522743.1:c.37+65A>G	XP_011521045.1:n.37+65A>G
XM_011522744.1:c.37+65A>G	XP_011521046.1:n.37+65A>G
XM_005255682.4:c.37+65A>G	XP_005255739.1:n.37+65A>G
XM_005255683.4:c.37+65A>G	XP_005255740.1:n.37+65A>G
XM_011522738.3:c.37+65A>G	XP_011521040.1:n.37+65A>G
XM_011522741.3:c.37+65A>G	XP_011521043.1:n.37+65A>G
XM_011522743.3:c.37+65A>G	XP_011521045.1:n.37+65A>G
XM_011522744.3:c.37+65A>G	XP_011521046.1:n.37+65A>G
XM_017023871.2:c.37+65A>G	XP_016879360.1:n.37+65A>G
XM_017023872.1:c.7+6962A>G	XP_016879361.1:n.7+6962A>G
XM_017023873.2:c.37+65A>G	XP_016879362.1:n.37+65A>G
XM_017023874.1:c.7+6962A>G	XP_016879363.1:n.7+6962A>G
XM_017023876.2:c.37+65A>G	XP_016879365.1:n.37+65A>G
XM_017023877.1:c.7+6962A>G	XP_016879366.1:n.7+6962A>G
XM_024450491.1:c.-269+6962A>G	XP_024306259.1:n.-269+6962A>G
XR_001752024.2:n.256+65A>G
NM_032167.5:c.7+6962A>G MANE Select	NP_115543.3:n.7+6962A>G
NM_001376490.1:c.7+6962A>G	NP_001363419.1:n.7+6962A>G