Canonical Allele Identifier: CA1873106765

Gene: SNX30

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.112788083A= , CM000671.2:g.112788083A=	GRCh38
NC_000009.11:g.115550363A= , CM000671.1:g.115550363A=	GRCh37
NC_000009.10:g.114590184A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001012994.2:c.157-16693A= MANE Select	NP_001013012.1:n.157-16693A=
ENST00000374232.8:c.157-16693A= MANE Select	ENSP00000363349.3:n.157-16693A=
NM_001012994.1:c.157-16693A=	NP_001013012.1:n.157-16693A=
ENST00000374232.7:c.157-16693A=	ENSP00000363349.3:n.157-16693A=
XM_005251986.3:c.-156-16693A=	XP_005252043.1:n.-156-16693A=
XM_011518691.1:c.157-16693A=	XP_011516993.1:n.157-16693A=
XM_011518691.2:c.157-16693A=	XP_011516993.1:n.157-16693A=
XM_017014716.2:c.34-16693A=	XP_016870205.1:n.34-16693A=
XM_024447544.1:c.-156-16693A=	XP_024303312.1:n.-156-16693A=