Canonical Allele Identifier: CA16523056

Gene: SNX20

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50680424G>A , CM000678.2:g.50680424G>A	GRCh38
NC_000016.9:g.50714335G>A , CM000678.1:g.50714335G>A	GRCh37
NC_000016.8:g.49271836G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330943.9:c.-10+766C>T MANE Select	ENSP00000332062.4:n.-10+766C>T
ENST00000300590.7:c.-10+766C>T	ENSP00000300590.3:n.-10+766C>T
ENST00000330943.8:c.-10+766C>T	ENSP00000332062.4:n.-10+766C>T
ENST00000423026.6:c.-10+766C>T	ENSP00000388875.2:n.-10+766C>T
ENST00000568993.5:c.-10+766C>T	ENSP00000454863.1:n.-10+766C>T
ENST00000610485.1:c.-10+766C>T	ENSP00000484863.1:n.-10+766C>T
NM_001144972.1:c.-10+766C>T	NP_001138444.1:n.-10+766C>T
NM_153337.2:c.-10+766C>T	NP_699168.1:n.-10+766C>T
NM_182854.2:c.-10+766C>T	NP_878274.1:n.-10+766C>T
NM_182854.3:c.-10+766C>T	NP_878274.1:n.-10+766C>T
NM_182854.4:c.-10+766C>T MANE Select	NP_878274.1:n.-10+766C>T
NM_001144972.2:c.-10+766C>T	NP_001138444.1:n.-10+766C>T
NM_153337.3:c.-10+766C>T	NP_699168.1:n.-10+766C>T