Canonical Allele Identifier: CA2806408338

Gene: SULT1A1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28606017_28606018insTA , CM000678.2:g.28606017_28606018insTA	GRCh38
NC_000016.9:g.28617338_28617339insTA , CM000678.1:g.28617338_28617339insTA	GRCh37
NC_000016.8:g.28524839_28524840insTA	NCBI36
NG_028128.1:g.22528_22529insTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314752.12:c.775+38_775+39insTA MANE Select	ENSP00000321988.7:n.775+38_775+39insTA
ENST00000395607.6:c.*1451+2690_*1451+2691insTA	ENSP00000378971.2:n.*1451+2690_*1451+2691insTA
ENST00000395609.6:n.2408+38_2408+39insTA
ENST00000677940.1:c.139-12450_139-12449insTA	ENSP00000503077.1:n.139-12450_139-12449insTA
ENST00000679262.1:c.*118+14045_*118+14046insTA	ENSP00000502863.1:n.*118+14045_*118+14046insTA
ENST00000314752.11:c.775+38_775+39insTA	ENSP00000321988.7:n.775+38_775+39insTA
ENST00000350842.8:c.541+38_541+39insTA	ENSP00000329399.4:n.541+38_541+39insTA
ENST00000395607.5:c.775+38_775+39insTA	ENSP00000378971.1:n.775+38_775+39insTA
ENST00000395609.5:c.775+38_775+39insTA	ENSP00000378972.1:n.775+38_775+39insTA
ENST00000562058.5:c.*1007+38_*1007+39insTA	ENSP00000456215.1:n.*1007+38_*1007+39insTA
ENST00000563493.1:c.*659+38_*659+39insTA	ENSP00000457083.1:n.*659+38_*659+39insTA
ENST00000564818.5:c.*1080+38_*1080+39insTA	ENSP00000454388.1:n.*1080+38_*1080+39insTA
ENST00000566189.5:c.775+38_775+39insTA	ENSP00000456459.1:n.775+38_775+39insTA
ENST00000567998.5:n.7605+38_7605+39insTA
ENST00000569554.5:c.775+38_775+39insTA	ENSP00000457912.1:n.775+38_775+39insTA
NM_001055.3:c.775+38_775+39insTA	NP_001046.2:n.775+38_775+39insTA
NM_177529.2:c.775+38_775+39insTA	NP_803565.1:n.775+38_775+39insTA
NM_177530.2:c.775+38_775+39insTA	NP_803566.1:n.775+38_775+39insTA
NM_177534.2:c.775+38_775+39insTA	NP_803878.1:n.775+38_775+39insTA
NM_177536.3:c.541+38_541+39insTA	NP_803880.1:n.541+38_541+39insTA
XM_017023604.1:c.793+38_793+39insTA	XP_016879093.1:n.793+38_793+39insTA
XM_017023605.1:c.793+38_793+39insTA	XP_016879094.1:n.793+38_793+39insTA
XM_017023607.2:c.1048+38_1048+39insTA	XP_016879096.1:n.1048+38_1048+39insTA
XM_017023608.1:c.793+38_793+39insTA	XP_016879097.1:n.793+38_793+39insTA
XM_017023609.1:c.793+38_793+39insTA	XP_016879098.1:n.793+38_793+39insTA
XM_017023610.1:c.793+38_793+39insTA	XP_016879099.1:n.793+38_793+39insTA
XM_017023611.2:c.775+38_775+39insTA	XP_016879100.1:n.775+38_775+39insTA
XM_017023612.2:c.775+38_775+39insTA	XP_016879101.1:n.775+38_775+39insTA
XM_017023613.2:c.775+38_775+39insTA	XP_016879102.1:n.775+38_775+39insTA
XM_024450408.1:c.1051+38_1051+39insTA	XP_024306176.1:n.1051+38_1051+39insTA
XM_024450409.1:c.775+38_775+39insTA	XP_024306177.1:n.775+38_775+39insTA
XM_024450410.1:c.775+38_775+39insTA	XP_024306178.1:n.775+38_775+39insTA
XM_024450411.1:c.775+38_775+39insTA	XP_024306179.1:n.775+38_775+39insTA
XR_001751973.1:n.1016+38_1016+39insTA
NM_177530.3:c.775+38_775+39insTA	NP_803566.1:n.775+38_775+39insTA
NM_177534.3:c.775+38_775+39insTA	NP_803878.1:n.775+38_775+39insTA
NM_177536.4:c.541+38_541+39insTA	NP_803880.1:n.541+38_541+39insTA
NM_001055.4:c.775+38_775+39insTA MANE Select	NP_001046.2:n.775+38_775+39insTA
NM_001394421.1:c.775+38_775+39insTA	NP_001381350.1:n.775+38_775+39insTA
NM_001394422.1:c.775+38_775+39insTA	NP_001381351.1:n.775+38_775+39insTA
NM_001394423.1:c.775+38_775+39insTA	NP_001381352.1:n.775+38_775+39insTA
NM_001394424.1:c.775+38_775+39insTA	NP_001381353.1:n.775+38_775+39insTA
NM_001394425.1:c.775+38_775+39insTA	NP_001381354.1:n.775+38_775+39insTA
NM_177529.3:c.775+38_775+39insTA	NP_803565.1:n.775+38_775+39insTA
NM_177530.4:c.775+38_775+39insTA	NP_803566.1:n.775+38_775+39insTA
NM_177534.4:c.775+38_775+39insTA	NP_803878.1:n.775+38_775+39insTA
NM_177536.5:c.472+38_472+39insTA	NP_803880.2:n.472+38_472+39insTA