Canonical Allele Identifier: CA6341630
Gene: SIAE HGNC NCBI

Linked Data

ClinVar Variation Id: 1168500
ClinVar RCV Id: RCV001518806
dbSNP Id: rs12282107

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.124669377T>C , CM000673.2:g.124669377T>C GRCh38
NC_000011.9:g.124539273T>C , CM000673.1:g.124539273T>C GRCh37
NC_000011.8:g.124044483T>C NCBI36
NG_028132.1:g.11927A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263593.8:c.212A>G MANE Select ENSP00000263593.3:p.Lys71Arg
ENST00000263593.7:c.212A>G ENSP00000263593.3:p.Lys71Arg
ENST00000436137.2:n.325A>G
ENST00000533613.1:n.236A>G
ENST00000545756.5:c.107A>G ENSP00000437877.1:p.Lys36Arg
ENST00000618733.4:c.107A>G ENSP00000478211.1:p.Lys36Arg
NM_001199922.1:c.107A>G NP_001186851.1:p.Lys36Arg
NM_170601.4:c.212A>G NP_733746.1:p.Lys71Arg
XM_005271592.3:c.212A>G XP_005271649.1:p.Lys71Arg
XM_017017930.1:c.-3041A>G XP_016873419.1:n.-3041A>G
NM_170601.5:c.212A>G MANE Select NP_733746.1:p.Lys71Arg
NM_001199922.2:c.107A>G NP_001186851.1:p.Lys36Arg