Canonical Allele Identifier: CA408634835
Gene: SNTA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33443605G>C , CM000682.2:g.33443605G>C GRCh38
NC_000020.10:g.32031411G>C , CM000682.1:g.32031411G>C GRCh37
NC_000020.9:g.31495072G>C NCBI36
NG_011622.1:g.5288C>G , LRG_332:g.5288C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.16C>G MANE Select ENSP00000217381.2:p.Arg6Gly
ENST00000217381.2:c.16C>G ENSP00000217381.2:p.Arg6Gly
NM_003098.2:c.16C>G , LRG_332t1:c.16C>G NP_003089.1:p.Arg6Gly
XM_005260517.1:c.16C>G XP_005260574.1:p.Arg6Gly
XM_011529007.1:c.16C>G XP_011527309.1:p.Arg6Gly
XM_011529008.1:c.16C>G XP_011527310.1:p.Arg6Gly
XR_936612.1:n.249C>G
NM_003098.3:c.16C>G MANE Select NP_003089.1:p.Arg6Gly