Canonical Allele Identifier: CA2277862931

Gene: CARD14 SGSH

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80211962_80211964delinsGAT , CM000679.2:g.80211962_80211964delinsGAT	GRCh38
NC_000017.10:g.78185761_78185763delinsGAT , CM000679.1:g.78185761_78185763delinsGAT	GRCh37
NC_000017.9:g.75800356_75800358delinsGAT	NCBI36
NG_008229.1:g.13437_13439delinsATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703570.1:n.2844+2704_2844+2706delinsGAT (CARD14)
ENST00000326317.11:c.949+107_949+109delinsATC (SGSH) MANE Select	ENSP00000314606.6:n.949+107_949+109delinsATC
ENST00000326317.10:c.949+107_949+109delinsATC (SGSH)	ENSP00000314606.6:n.949+107_949+109delinsATC
ENST00000570923.1:c.*266_*268delinsATC (SGSH)	ENSP00000458200.1:n.*266_*268delinsATC
ENST00000572257.5:c.551+107_551+109delinsATC (SGSH)
ENST00000573150.5:c.*159+107_*159+109delinsATC (SGSH)	ENSP00000459280.1:n.*159+107_*159+109delinsATC
ENST00000575282.5:n.2880_2882delinsATC (SGSH)
ENST00000576856.1:c.149-41_149-39delinsATC (SGSH)	ENSP00000460720.1:n.149-41_149-39delinsATC
NM_000199.3:c.949+107_949+109delinsATC (SGSH)	NP_000190.1:n.949+107_949+109delinsATC
XM_005257582.2:c.949+107_949+109delinsATC (SGSH)	XP_005257639.1:n.949+107_949+109delinsATC
XM_005257583.3:c.949+107_949+109delinsATC (SGSH)	XP_005257640.1:n.949+107_949+109delinsATC
XM_011525126.1:c.950-41_950-39delinsATC (SGSH)	XP_011523428.1:n.950-41_950-39delinsATC
XM_011525127.1:c.950-41_950-39delinsATC (SGSH)	XP_011523429.1:n.950-41_950-39delinsATC
XR_934532.1:n.1076_1078delinsATC (SGSH)
NM_000199.4:c.949+107_949+109delinsATC (SGSH)	NP_000190.1:n.949+107_949+109delinsATC
NM_001352921.1:c.949+107_949+109delinsATC (SGSH)	NP_001339850.1:n.949+107_949+109delinsATC
NM_001352922.1:c.950-41_950-39delinsATC (SGSH)	NP_001339851.1:n.950-41_950-39delinsATC
NR_148201.1:n.930+107_930+109delinsATC (SGSH)
XM_005257583.4:c.949+107_949+109delinsATC (SGSH)	XP_005257640.1:n.949+107_949+109delinsATC
XM_017024952.1:c.950-41_950-39delinsATC (SGSH)	XP_016880441.1:n.950-41_950-39delinsATC
XR_001752585.1:n.969+107_969+109delinsATC (SGSH)
XR_001752586.1:n.969+107_969+109delinsATC (SGSH)
XR_001752587.1:n.969+107_969+109delinsATC (SGSH)
XR_001752588.1:n.969+107_969+109delinsATC (SGSH)
XR_001752589.1:n.969+107_969+109delinsATC (SGSH)
XR_001752590.1:n.969+107_969+109delinsATC (SGSH)
XR_001752591.1:n.969+107_969+109delinsATC (SGSH)
XR_001752592.1:n.969+107_969+109delinsATC (SGSH)
XR_002958057.1:n.970-41_970-39delinsATC (SGSH)
XR_934532.2:n.1076_1078delinsATC (SGSH)
NM_000199.5:c.949+107_949+109delinsATC (SGSH) MANE Select	NP_000190.1:n.949+107_949+109delinsATC
NM_001352921.2:c.949+107_949+109delinsATC (SGSH)	NP_001339850.1:n.949+107_949+109delinsATC
NM_001352922.2:c.950-41_950-39delinsATC (SGSH)	NP_001339851.1:n.950-41_950-39delinsATC
NR_148201.2:n.863+107_863+109delinsATC (SGSH)
NM_001352921.3:c.949+107_949+109delinsATC (SGSH)	NP_001339850.1:n.949+107_949+109delinsATC