Canonical Allele Identifier: CA393128710
Gene: STRA6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74180782C>G , CM000677.2:g.74180782C>G GRCh38
NC_000015.9:g.74473123C>G , CM000677.1:g.74473123C>G GRCh37
NC_000015.8:g.72260176C>G NCBI36
NG_009207.1:g.33249G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000395105.9:c.1840G>C MANE Select ENSP00000378537.4:p.Gly614Arg
ENST00000323940.9:c.1840G>C ENSP00000326085.5:p.Gly614Arg
ENST00000395105.8:c.1840G>C ENSP00000378537.4:p.Gly614Arg
ENST00000416286.7:c.1816G>C ENSP00000400403.3:p.Gly606Arg
ENST00000423167.6:c.1813G>C ENSP00000413012.2:p.Gly605Arg
ENST00000449139.6:c.1840G>C ENSP00000410221.2:p.Gly614Arg
ENST00000535552.5:c.1951G>C ENSP00000440238.1:p.Gly651Arg
ENST00000545137.5:n.1549G>C
ENST00000563965.5:c.1957G>C ENSP00000456609.1:p.Gly653Arg
ENST00000572785.1:c.695G>C
ENST00000574278.5:c.1885G>C ENSP00000458827.1:p.Gly629Arg
ENST00000574439.5:n.2112G>C
ENST00000616000.4:c.1840G>C ENSP00000479112.1:p.Gly614Arg
NM_001142617.1:c.1840G>C NP_001136089.1:p.Gly614Arg
NM_001142618.1:c.1840G>C NP_001136090.1:p.Gly614Arg
NM_001142619.1:c.1813G>C NP_001136091.1:p.Gly605Arg
NM_001199040.1:c.1951G>C NP_001185969.1:p.Gly651Arg
NM_001199041.1:c.1885G>C NP_001185970.1:p.Gly629Arg
NM_001199042.1:c.1957G>C NP_001185971.1:p.Gly653Arg
NM_022369.3:c.1840G>C NP_071764.3:p.Gly614Arg
XM_011521883.1:c.1840G>C XP_011520185.1:p.Gly614Arg
XM_011521884.1:c.1651G>C XP_011520186.1:p.Gly551Arg
XM_017022478.1:c.1888G>C XP_016877967.1:p.Gly630Arg
XM_017022479.1:c.1840G>C XP_016877968.1:p.Gly614Arg
XM_017022480.1:c.1651G>C XP_016877969.1:p.Gly551Arg
NM_022369.4:c.1840G>C MANE Select NP_071764.3:p.Gly614Arg
NM_001142617.2:c.1840G>C NP_001136089.1:p.Gly614Arg
NM_001142619.2:c.1813G>C NP_001136091.1:p.Gly605Arg
NM_001199042.2:c.1957G>C NP_001185971.1:p.Gly653Arg
NM_001142618.2:c.1840G>C NP_001136090.1:p.Gly614Arg
NM_001199040.2:c.1951G>C NP_001185969.1:p.Gly651Arg
NM_001199041.2:c.1885G>C NP_001185970.1:p.Gly629Arg