Canonical Allele Identifier: CA2558262252

Gene: SNX30

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.112788112G>T , CM000671.2:g.112788112G>T	GRCh38
NC_000009.11:g.115550392G>T , CM000671.1:g.115550392G>T	GRCh37
NC_000009.10:g.114590213G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374232.8:c.157-16664G>T MANE Select	ENSP00000363349.3:n.157-16664G>T
ENST00000374232.7:c.157-16664G>T	ENSP00000363349.3:n.157-16664G>T
NM_001012994.1:c.157-16664G>T	NP_001013012.1:n.157-16664G>T
XM_005251986.3:c.-156-16664G>T	XP_005252043.1:n.-156-16664G>T
XM_011518691.1:c.157-16664G>T	XP_011516993.1:n.157-16664G>T
XM_011518691.2:c.157-16664G>T	XP_011516993.1:n.157-16664G>T
XM_017014716.2:c.34-16664G>T	XP_016870205.1:n.34-16664G>T
XM_024447544.1:c.-156-16664G>T	XP_024303312.1:n.-156-16664G>T
NM_001012994.2:c.157-16664G>T MANE Select	NP_001013012.1:n.157-16664G>T