Canonical Allele Identifier: CA2277863892

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80213878_80213879delinsTA , CM000679.2:g.80213878_80213879delinsTA GRCh38
NC_000017.10:g.78187677_78187678delinsTA , CM000679.1:g.78187677_78187678delinsTA GRCh37
NC_000017.9:g.75802272_75802273delinsTA NCBI36
NG_008229.1:g.11522_11523delinsTA

Transcript Alleles

HGVS Amino-acid change
ENST00000703570.1:n.2845-1988_2845-1987delinsTA (CARD14)
ENST00000326317.11:c.670_671delinsTA (SGSH) MANE Select ENSP00000314606.6:p.Tyr224=
ENST00000326317.10:c.670_671delinsTA (SGSH) ENSP00000314606.6:p.Tyr224=
ENST00000570923.1:c.705_706delinsTA (SGSH) ENSP00000458200.1:p.Leu235=
ENST00000572208.5:n.537_538delinsTA (SGSH)
ENST00000572257.5:c.272_273delinsTA (SGSH)
ENST00000573150.5:c.564_565delinsTA (SGSH) ENSP00000459280.1:p.Leu188=
ENST00000574505.5:c.529_530delinsTA (SGSH)
ENST00000575282.5:n.965_966delinsTA (SGSH)
ENST00000576941.5:c.*86_*87delinsTA (SGSH) ENSP00000461160.1:n.*86_*87delinsTA
NM_000199.3:c.670_671delinsTA (SGSH) NP_000190.1:p.Tyr224=
XM_005257582.2:c.670_671delinsTA (SGSH) XP_005257639.1:p.Tyr224=
XM_005257583.3:c.670_671delinsTA (SGSH) XP_005257640.1:p.Tyr224=
XM_011525126.1:c.670_671delinsTA (SGSH) XP_011523428.1:p.Tyr224=
XM_011525127.1:c.670_671delinsTA (SGSH) XP_011523429.1:p.Tyr224=
XR_934532.1:n.690_691delinsTA (SGSH)
NM_000199.4:c.670_671delinsTA (SGSH) NP_000190.1:p.Tyr224=
NM_001352921.1:c.670_671delinsTA (SGSH) NP_001339850.1:p.Tyr224=
NM_001352922.1:c.670_671delinsTA (SGSH) NP_001339851.1:p.Tyr224=
NR_148201.1:n.651_652delinsTA (SGSH)
XM_005257583.4:c.670_671delinsTA (SGSH) XP_005257640.1:p.Tyr224=
XM_017024952.1:c.670_671delinsTA (SGSH) XP_016880441.1:p.Tyr224=
XR_001752585.1:n.690_691delinsTA (SGSH)
XR_001752586.1:n.690_691delinsTA (SGSH)
XR_001752587.1:n.690_691delinsTA (SGSH)
XR_001752588.1:n.690_691delinsTA (SGSH)
XR_001752589.1:n.690_691delinsTA (SGSH)
XR_001752590.1:n.690_691delinsTA (SGSH)
XR_001752591.1:n.690_691delinsTA (SGSH)
XR_001752592.1:n.690_691delinsTA (SGSH)
XR_002958057.1:n.690_691delinsTA (SGSH)
XR_934532.2:n.690_691delinsTA (SGSH)
NM_000199.5:c.670_671delinsTA (SGSH) MANE Select NP_000190.1:p.Tyr224=
NM_001352921.2:c.670_671delinsTA (SGSH) NP_001339850.1:p.Tyr224=
NM_001352922.2:c.670_671delinsTA (SGSH) NP_001339851.1:p.Tyr224=
NR_148201.2:n.584_585delinsTA (SGSH)
NM_001352921.3:c.670_671delinsTA (SGSH) NP_001339850.1:p.Tyr224=