Canonical Allele Identifier: CA2360740071
Gene: SNTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33408526_33408527delinsCG , CM000682.2:g.33408526_33408527delinsCG GRCh38
NC_000020.10:g.31996332_31996333delinsCG , CM000682.1:g.31996332_31996333delinsCG GRCh37
NC_000020.9:g.31459993_31459994delinsCG NCBI36
NG_011622.1:g.40366_40367delinsCG , LRG_332:g.40366_40367delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.1498_1499delinsCG MANE Select ENSP00000217381.2:p.Arg500=
ENST00000217381.2:c.1498_1499delinsCG ENSP00000217381.2:p.Arg500=
NM_003098.2:c.1498_1499delinsCG , LRG_332t1:c.1498_1499delinsCG NP_003089.1:p.Arg500=
XM_005260517.1:c.1495_1496delinsCG XP_005260574.1:p.Arg499=
XM_011529007.1:c.*39_*40delinsCG XP_011527309.1:n.*39_*40delinsCG
XM_011529008.1:c.*39_*40delinsCG XP_011527310.1:n.*39_*40delinsCG
XR_936612.1:n.1534_1535delinsCG
XM_024451971.1:c.1171_1172delinsCG XP_024307739.1:p.Arg391=
NM_003098.3:c.1498_1499delinsCG MANE Select NP_003089.1:p.Arg500=