Canonical Allele Identifier: CA1873106804

Gene: SNX30

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.112788157_112788158delinsGA , CM000671.2:g.112788157_112788158delinsGA	GRCh38
NC_000009.11:g.115550437_115550438delinsGA , CM000671.1:g.115550437_115550438delinsGA	GRCh37
NC_000009.10:g.114590258_114590259delinsGA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374232.8:c.157-16619_157-16618delinsGA MANE Select	ENSP00000363349.3:n.157-16619_157-16618delinsGA
ENST00000374232.7:c.157-16619_157-16618delinsGA	ENSP00000363349.3:n.157-16619_157-16618delinsGA
NM_001012994.1:c.157-16619_157-16618delinsGA	NP_001013012.1:n.157-16619_157-16618delinsGA
XM_005251986.3:c.-156-16619_-156-16618delinsGA	XP_005252043.1:n.-156-16619_-156-16618delinsGA
XM_011518691.1:c.157-16619_157-16618delinsGA	XP_011516993.1:n.157-16619_157-16618delinsGA
XM_011518691.2:c.157-16619_157-16618delinsGA	XP_011516993.1:n.157-16619_157-16618delinsGA
XM_017014716.2:c.34-16619_34-16618delinsGA	XP_016870205.1:n.34-16619_34-16618delinsGA
XM_024447544.1:c.-156-16619_-156-16618delinsGA	XP_024303312.1:n.-156-16619_-156-16618delinsGA
NM_001012994.2:c.157-16619_157-16618delinsGA MANE Select	NP_001013012.1:n.157-16619_157-16618delinsGA