Canonical Allele Identifier: CA1128238529

Gene: SNX30

Linked Data

• dbSNP Id: rs1839961653
• gnomAD v3: 9-112788157-GA-G
• gnomAD v4: 9-112788157-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.112788159del , CM000671.2:g.112788159del	GRCh38
NC_000009.11:g.115550439del , CM000671.1:g.115550439del	GRCh37
NC_000009.10:g.114590260del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374232.8:c.157-16617del MANE Select	ENSP00000363349.3:n.157-16617del
ENST00000374232.7:c.157-16617del	ENSP00000363349.3:n.157-16617del
NM_001012994.1:c.157-16617del	NP_001013012.1:n.157-16617del
XM_005251986.3:c.-156-16617del	XP_005252043.1:n.-156-16617del
XM_011518691.1:c.157-16617del	XP_011516993.1:n.157-16617del
XM_011518691.2:c.157-16617del	XP_011516993.1:n.157-16617del
XM_017014716.2:c.34-16617del	XP_016870205.1:n.34-16617del
XM_024447544.1:c.-156-16617del	XP_024303312.1:n.-156-16617del
NM_001012994.2:c.157-16617del MANE Select	NP_001013012.1:n.157-16617del