Canonical Allele Identifier: CA2632511463

Gene: SULT1A1

Linked Data

• dbSNP Id: rs2151699179
• gnomAD v4: 16-28609476-GCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28609479_28609480del , CM000678.2:g.28609479_28609480del	GRCh38
NC_000016.9:g.28620800_28620801del , CM000678.1:g.28620800_28620801del	GRCh37
NC_000016.8:g.28528301_28528302del	NCBI36
NG_028128.1:g.19068_19069del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314752.12:c.-5+453_-5+454del MANE Select	ENSP00000321988.7:n.-5+453_-5+454del
ENST00000395607.6:c.*681_*682del	ENSP00000378971.2:n.*681_*682del
ENST00000395609.6:n.1210_1211del
ENST00000677940.1:c.138+10585_138+10586del	ENSP00000503077.1:n.138+10585_138+10586del
ENST00000679262.1:c.*118+10585_*118+10586del	ENSP00000502863.1:n.*118+10585_*118+10586del
ENST00000314752.11:c.-5+453_-5+454del	ENSP00000321988.7:n.-5+453_-5+454del
ENST00000350842.8:c.139-2401_139-2400del	ENSP00000329399.4:n.139-2401_139-2400del
ENST00000395609.5:c.-5+453_-5+454del	ENSP00000378972.1:n.-5+453_-5+454del
ENST00000562058.5:c.*228+453_*228+454del	ENSP00000456215.1:n.*228+453_*228+454del
ENST00000563493.1:c.139-619_139-618del	ENSP00000457083.1:n.139-619_139-618del
ENST00000564818.5:c.*229-43_*229-42del	ENSP00000454388.1:n.*229-43_*229-42del
ENST00000566189.5:c.-36+453_-36+454del	ENSP00000456459.1:n.-36+453_-36+454del
ENST00000567512.1:c.-5+453_-5+454del	ENSP00000455979.1:n.-5+453_-5+454del
ENST00000567998.5:n.4802_4803del
NM_001055.3:c.-5+453_-5+454del	NP_001046.2:n.-5+453_-5+454del
NM_177529.2:c.-36+453_-36+454del	NP_803565.1:n.-36+453_-36+454del
NM_177536.3:c.139-2401_139-2400del	NP_803880.1:n.139-2401_139-2400del
XM_017023604.1:c.-80-40_-80-39del	XP_016879093.1:n.-80-40_-80-39del
XM_017023605.1:c.-77-43_-77-42del	XP_016879094.1:n.-77-43_-77-42del
XM_017023607.2:c.197-43_197-42del	XP_016879096.1:n.197-43_197-42del
XM_017023608.1:c.-5+453_-5+454del	XP_016879097.1:n.-5+453_-5+454del
XM_017023611.2:c.-5+453_-5+454del	XP_016879100.1:n.-5+453_-5+454del
XM_017023612.2:c.-5+453_-5+454del	XP_016879101.1:n.-5+453_-5+454del
XM_017023613.2:c.-4-619_-4-618del	XP_016879102.1:n.-4-619_-4-618del
XM_024450408.1:c.197-40_197-39del	XP_024306176.1:n.197-40_197-39del
XM_024450409.1:c.-455_-454del	XP_024306177.1:n.-455_-454del
XM_024450410.1:c.-583-40_-583-39del	XP_024306178.1:n.-583-40_-583-39del
XM_024450411.1:c.-424_-423del	XP_024306179.1:n.-424_-423del
XR_001751973.1:n.124-40_124-39del
NM_177536.4:c.139-2401_139-2400del	NP_803880.1:n.139-2401_139-2400del
NM_001055.4:c.-5+453_-5+454del MANE Select	NP_001046.2:n.-5+453_-5+454del
NM_001394421.1:c.-77-43_-77-42del	NP_001381350.1:n.-77-43_-77-42del
NM_001394422.1:c.-424_-423del	NP_001381351.1:n.-424_-423del
NM_001394423.1:c.-77-43_-77-42del	NP_001381352.1:n.-77-43_-77-42del
NM_001394424.1:c.-35-588_-35-587del	NP_001381353.1:n.-35-588_-35-587del
NM_001394425.1:c.-5+453_-5+454del	NP_001381354.1:n.-5+453_-5+454del
NM_177529.3:c.-36+453_-36+454del	NP_803565.1:n.-36+453_-36+454del
NM_177530.4:c.-424_-423del	NP_803566.1:n.-424_-423del
NM_177534.4:c.-623_-622del	NP_803878.1:n.-623_-622del
NM_177536.5:c.70-2401_70-2400del	NP_803880.2:n.70-2401_70-2400del