Canonical Allele Identifier: CA393128279
Gene: STRA6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74180151G>C , CM000677.2:g.74180151G>C GRCh38
NC_000015.9:g.74472492G>C , CM000677.1:g.74472492G>C GRCh37
NC_000015.8:g.72259545G>C NCBI36
NG_009207.1:g.33880C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000395105.9:c.1933C>G MANE Select ENSP00000378537.4:p.Leu645Val
ENST00000323940.9:c.1933C>G ENSP00000326085.5:p.Leu645Val
ENST00000395105.8:c.1933C>G ENSP00000378537.4:p.Leu645Val
ENST00000416286.7:c.1909C>G ENSP00000400403.3:p.Leu637Val
ENST00000423167.6:c.1906C>G ENSP00000413012.2:p.Leu636Val
ENST00000449139.6:c.1933C>G ENSP00000410221.2:p.Leu645Val
ENST00000535552.5:c.2044C>G ENSP00000440238.1:p.Leu682Val
ENST00000545137.5:n.1642C>G
ENST00000563965.5:c.2050C>G ENSP00000456609.1:p.Leu684Val
ENST00000572785.1:c.788C>G
ENST00000574278.5:c.1978C>G ENSP00000458827.1:p.Leu660Val
ENST00000574439.5:n.2205C>G
ENST00000616000.4:c.1933C>G ENSP00000479112.1:p.Leu645Val
NM_001142617.1:c.1933C>G NP_001136089.1:p.Leu645Val
NM_001142618.1:c.1933C>G NP_001136090.1:p.Leu645Val
NM_001142619.1:c.1906C>G NP_001136091.1:p.Leu636Val
NM_001199040.1:c.2044C>G NP_001185969.1:p.Leu682Val
NM_001199041.1:c.1978C>G NP_001185970.1:p.Leu660Val
NM_001199042.1:c.2050C>G NP_001185971.1:p.Leu684Val
NM_022369.3:c.1933C>G NP_071764.3:p.Leu645Val
XM_011521883.1:c.1933C>G XP_011520185.1:p.Leu645Val
XM_011521884.1:c.1744C>G XP_011520186.1:p.Leu582Val
XM_017022478.1:c.1981C>G XP_016877967.1:p.Leu661Val
XM_017022479.1:c.1933C>G XP_016877968.1:p.Leu645Val
XM_017022480.1:c.1744C>G XP_016877969.1:p.Leu582Val
NM_022369.4:c.1933C>G MANE Select NP_071764.3:p.Leu645Val
NM_001142617.2:c.1933C>G NP_001136089.1:p.Leu645Val
NM_001142619.2:c.1906C>G NP_001136091.1:p.Leu636Val
NM_001199042.2:c.2050C>G NP_001185971.1:p.Leu684Val
NM_001142618.2:c.1933C>G NP_001136090.1:p.Leu645Val
NM_001199040.2:c.2044C>G NP_001185969.1:p.Leu682Val
NM_001199041.2:c.1978C>G NP_001185970.1:p.Leu660Val