Canonical Allele Identifier: CA721365315

Gene: SNX20

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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