Canonical Allele Identifier: CA294883741

Gene: CARD14 SGSH

Linked Data

• dbSNP Id: rs867829696
• gnomAD v2: 17-78179404-G-A
• gnomAD v4: 17-80205605-G-A
• MyVariant Identifiers: chr17:g.78179404G>A (hg19) ; chr17:g.80205605G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80205605G>A , CM000679.2:g.80205605G>A	GRCh38
NC_000017.10:g.78179404G>A , CM000679.1:g.78179404G>A	GRCh37
NC_000017.9:g.75793999G>A	NCBI36
NG_032778.1:g.40614G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000571427.2:c.2644G>A (CARD14)	ENSP00000516501.1:p.Gly882Ser
ENST00000703566.1:c.*480G>A (CARD14)	ENSP00000515382.1:n.*480G>A
ENST00000703567.1:c.*480G>A (CARD14)	ENSP00000515383.1:n.*480G>A
ENST00000703568.1:c.*1104G>A (CARD14)	ENSP00000515384.1:n.*1104G>A
ENST00000703569.1:n.2845G>A (CARD14)
ENST00000703570.1:n.1560G>A (CARD14)
ENST00000703571.1:n.1492G>A (CARD14)
ENST00000703572.1:n.528G>A (CARD14)
ENST00000703573.1:n.862G>A (CARD14)
ENST00000648509.2:c.2644G>A (CARD14) MANE Select	ENSP00000498071.1:p.Gly882Ser
ENST00000649277.1:n.1401G>A (CARD14)
ENST00000650867.1:c.*89G>A (CARD14)	ENSP00000498570.1:n.*89G>A
ENST00000651068.1:c.*1003G>A (CARD14)	ENSP00000498274.1:n.*1003G>A
ENST00000651672.1:c.2671G>A (CARD14)	ENSP00000499145.1:p.Gly891Ser
ENST00000344227.6:c.2644G>A (CARD14)	ENSP00000344549.2:p.Gly882Ser
ENST00000573882.5:c.2644G>A (CARD14)	ENSP00000458715.1:p.Gly882Ser
ENST00000575500.5:c.*1104G>A (CARD14)	ENSP00000460883.1:n.*1104G>A
NM_024110.4:c.2644G>A (CARD14)	NP_077015.2:p.Gly882Ser
NR_047566.1:n.2819G>A (CARD14)
XM_011525212.1:c.2644G>A (CARD14)	XP_011523514.1:p.Gly882Ser
XM_011525213.1:c.2644G>A (CARD14)	XP_011523515.1:p.Gly882Ser
XM_011525214.1:c.2644G>A (CARD14)	XP_011523516.1:p.Gly882Ser
XM_011525215.1:c.2644G>A (CARD14)	XP_011523517.1:p.Gly882Ser
XM_011525216.1:c.2644G>A (CARD14)	XP_011523518.1:p.Gly882Ser
XM_011525217.1:c.2644G>A (CARD14)	XP_011523519.1:p.Gly882Ser
XM_011525218.1:c.2644G>A (CARD14)	XP_011523520.1:p.Gly882Ser
XM_011525219.1:c.*89G>A (CARD14)	XP_011523521.1:n.*89G>A
NM_001366385.1:c.2644G>A (CARD14) MANE Select	NP_001353314.1:p.Gly882Ser
XM_011525218.2:c.2644G>A (CARD14)	XP_011523520.1:p.Gly882Ser
XM_024450934.1:c.2641G>A (CARD14)	XP_024306702.1:p.Gly881Ser
XM_024450935.1:c.2644G>A (CARD14)	XP_024306703.1:p.Gly882Ser
XR_001752586.1:n.1491C>T (SGSH)
XR_001752587.1:n.1298C>T (SGSH)
XR_001752588.1:n.1491C>T (SGSH)
XR_001752589.1:n.1491C>T (SGSH)
XR_001752590.1:n.1491C>T (SGSH)
XR_001752591.1:n.1491C>T (SGSH)
XR_001752592.1:n.1491C>T (SGSH)
XR_002958057.1:n.2088C>T (SGSH)
XR_002958065.1:n.2794G>A (CARD14)
NR_047566.2:n.2781G>A (CARD14)