Canonical Allele Identifier: CA2277859638

Gene: CARD14 SGSH

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80205454_80205456delinsCAG , CM000679.2:g.80205454_80205456delinsCAG	GRCh38
NC_000017.10:g.78179253_78179255delinsCAG , CM000679.1:g.78179253_78179255delinsCAG	GRCh37
NC_000017.9:g.75793848_75793850delinsCAG	NCBI36
NG_032778.1:g.40463_40465delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000571427.2:c.2570-77_2570-75delinsCAG (CARD14)	ENSP00000516501.1:n.2570-77_2570-75delinsCAG
ENST00000703566.1:c.*406-77_*406-75delinsCAG (CARD14)	ENSP00000515382.1:n.*406-77_*406-75delinsCAG
ENST00000703567.1:c.*406-77_*406-75delinsCAG (CARD14)	ENSP00000515383.1:n.*406-77_*406-75delinsCAG
ENST00000703568.1:c.*1030-77_*1030-75delinsCAG (CARD14)	ENSP00000515384.1:n.*1030-77_*1030-75delinsCAG
ENST00000703569.1:n.2771-77_2771-75delinsCAG (CARD14)
ENST00000703570.1:n.1486-77_1486-75delinsCAG (CARD14)
ENST00000703571.1:n.1418-77_1418-75delinsCAG (CARD14)
ENST00000703572.1:n.454-77_454-75delinsCAG (CARD14)
ENST00000703573.1:n.788-77_788-75delinsCAG (CARD14)
ENST00000648509.2:c.2570-77_2570-75delinsCAG (CARD14) MANE Select	ENSP00000498071.1:n.2570-77_2570-75delinsCAG
ENST00000649277.1:n.1327-77_1327-75delinsCAG (CARD14)
ENST00000650867.1:c.*15-77_*15-75delinsCAG (CARD14)	ENSP00000498570.1:n.*15-77_*15-75delinsCAG
ENST00000651068.1:c.*929-77_*929-75delinsCAG (CARD14)	ENSP00000498274.1:n.*929-77_*929-75delinsCAG
ENST00000651672.1:c.2597-77_2597-75delinsCAG (CARD14)	ENSP00000499145.1:n.2597-77_2597-75delinsCAG
ENST00000344227.6:c.2570-77_2570-75delinsCAG (CARD14)	ENSP00000344549.2:n.2570-77_2570-75delinsCAG
ENST00000573882.5:c.2570-77_2570-75delinsCAG (CARD14)	ENSP00000458715.1:n.2570-77_2570-75delinsCAG
ENST00000575500.5:c.*1030-77_*1030-75delinsCAG (CARD14)	ENSP00000460883.1:n.*1030-77_*1030-75delinsCAG
NM_024110.4:c.2570-77_2570-75delinsCAG (CARD14)	NP_077015.2:n.2570-77_2570-75delinsCAG
NR_047566.1:n.2745-77_2745-75delinsCAG (CARD14)
XM_011525212.1:c.2570-77_2570-75delinsCAG (CARD14)	XP_011523514.1:n.2570-77_2570-75delinsCAG
XM_011525213.1:c.2570-77_2570-75delinsCAG (CARD14)	XP_011523515.1:n.2570-77_2570-75delinsCAG
XM_011525214.1:c.2570-77_2570-75delinsCAG (CARD14)	XP_011523516.1:n.2570-77_2570-75delinsCAG
XM_011525215.1:c.2570-77_2570-75delinsCAG (CARD14)	XP_011523517.1:n.2570-77_2570-75delinsCAG
XM_011525216.1:c.2570-77_2570-75delinsCAG (CARD14)	XP_011523518.1:n.2570-77_2570-75delinsCAG
XM_011525217.1:c.2570-77_2570-75delinsCAG (CARD14)	XP_011523519.1:n.2570-77_2570-75delinsCAG
XM_011525218.1:c.2570-77_2570-75delinsCAG (CARD14)	XP_011523520.1:n.2570-77_2570-75delinsCAG
XM_011525219.1:c.*15-77_*15-75delinsCAG (CARD14)	XP_011523521.1:n.*15-77_*15-75delinsCAG
NM_001366385.1:c.2570-77_2570-75delinsCAG (CARD14) MANE Select	NP_001353314.1:n.2570-77_2570-75delinsCAG
XM_011525218.2:c.2570-77_2570-75delinsCAG (CARD14)	XP_011523520.1:n.2570-77_2570-75delinsCAG
XM_024450934.1:c.2567-77_2567-75delinsCAG (CARD14)	XP_024306702.1:n.2567-77_2567-75delinsCAG
XM_024450935.1:c.2570-77_2570-75delinsCAG (CARD14)	XP_024306703.1:n.2570-77_2570-75delinsCAG
XR_001752586.1:n.1640_1642delinsCTG (SGSH)
XR_001752587.1:n.1447_1449delinsCTG (SGSH)
XR_001752588.1:n.1640_1642delinsCTG (SGSH)
XR_001752589.1:n.1640_1642delinsCTG (SGSH)
XR_001752590.1:n.1640_1642delinsCTG (SGSH)
XR_001752591.1:n.1640_1642delinsCTG (SGSH)
XR_001752592.1:n.1572-22_1572-20delinsCTG (SGSH)
XR_002958057.1:n.2237_2239delinsCTG (SGSH)
XR_002958065.1:n.2720-77_2720-75delinsCAG (CARD14)
NR_047566.2:n.2707-77_2707-75delinsCAG (CARD14)