Canonical Allele Identifier: CA8817482

Gene: CARD14 SGSH

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80208119C>A , CM000679.2:g.80208119C>A	GRCh38
NC_000017.10:g.78181918C>A , CM000679.1:g.78181918C>A	GRCh37
NC_000017.9:g.75796513C>A	NCBI36
NG_008229.1:g.17282G>T
NG_032778.1:g.43128C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001366385.1:c.2808-19C>A (CARD14) MANE Select	NP_001353314.1:n.2808-19C>A
ENST00000648509.2:c.2808-19C>A (CARD14) MANE Select	ENSP00000498071.1:n.2808-19C>A
NM_024110.4:c.2808-19C>A (CARD14)	NP_077015.2:n.2808-19C>A
NR_047566.1:n.2983-19C>A (CARD14)
NR_047566.2:n.2945-19C>A (CARD14)
ENST00000344227.6:c.2808-19C>A (CARD14)	ENSP00000344549.2:n.2808-19C>A
ENST00000571156.1:n.474-434G>T (SGSH)
ENST00000571427.2:c.2808-19C>A (CARD14)	ENSP00000516501.1:n.2808-19C>A
ENST00000572257.5:c.552-434G>T (SGSH)
ENST00000573882.5:c.2808-19C>A (CARD14)	ENSP00000458715.1:n.2808-19C>A
ENST00000575484.1:n.138-434G>T (SGSH)
ENST00000575500.5:c.*1268-19C>A (CARD14)	ENSP00000460883.1:n.*1268-19C>A
ENST00000649277.1:n.1565-19C>A (CARD14)
ENST00000650867.1:c.*253-19C>A (CARD14)	ENSP00000498570.1:n.*253-19C>A
ENST00000651068.1:c.*1167-19C>A (CARD14)	ENSP00000498274.1:n.*1167-19C>A
ENST00000651672.1:c.2835-19C>A (CARD14)	ENSP00000499145.1:n.2835-19C>A
ENST00000703566.1:c.*644-19C>A (CARD14)	ENSP00000515382.1:n.*644-19C>A
ENST00000703567.1:c.*644-19C>A (CARD14)	ENSP00000515383.1:n.*644-19C>A
ENST00000703568.1:c.*1268-19C>A (CARD14)	ENSP00000515384.1:n.*1268-19C>A
ENST00000703569.1:n.3009-19C>A (CARD14)
ENST00000703570.1:n.1724-19C>A (CARD14)
ENST00000703572.1:n.692-19C>A (CARD14)
ENST00000703573.1:n.1026-19C>A (CARD14)
XM_005257583.3:c.950-434G>T (SGSH)	XP_005257640.1:n.950-434G>T
XM_005257583.4:c.950-434G>T (SGSH)	XP_005257640.1:n.950-434G>T
XM_011525212.1:c.2808-19C>A (CARD14)	XP_011523514.1:n.2808-19C>A
XM_011525213.1:c.2808-19C>A (CARD14)	XP_011523515.1:n.2808-19C>A
XM_011525214.1:c.2808-19C>A (CARD14)	XP_011523516.1:n.2808-19C>A
XM_011525215.1:c.2808-19C>A (CARD14)	XP_011523517.1:n.2808-19C>A
XM_011525216.1:c.2808-19C>A (CARD14)	XP_011523518.1:n.2808-19C>A
XM_011525217.1:c.2808-19C>A (CARD14)	XP_011523519.1:n.2808-19C>A
XM_011525218.1:c.2808-19C>A (CARD14)	XP_011523520.1:n.2808-19C>A
XM_011525218.2:c.2808-19C>A (CARD14)	XP_011523520.1:n.2808-19C>A
XM_024450934.1:c.2805-19C>A (CARD14)	XP_024306702.1:n.2805-19C>A
XR_001752585.1:n.2580-434G>T (SGSH)
XR_001752586.1:n.970-434G>T (SGSH)
XR_001752587.1:n.970-434G>T (SGSH)
XR_001752588.1:n.970-434G>T (SGSH)
XR_001752589.1:n.970-434G>T (SGSH)
XR_001752590.1:n.970-434G>T (SGSH)
XR_001752591.1:n.970-434G>T (SGSH)
XR_001752592.1:n.970-434G>T (SGSH)
XR_002958057.1:n.1025-434G>T (SGSH)
XR_002958065.1:n.2958-19C>A (CARD14)