Canonical Allele Identifier: CA294890158

Gene: CARD14 SGSH

Linked Data

• dbSNP Id: rs978443728
• gnomAD v2: 17-78184034-C-T
• gnomAD v3: 17-80210235-C-T
• gnomAD v4: 17-80210235-C-T
• MyVariant Identifiers: chr17:g.78184034C>T (hg19) ; chr17:g.80210235C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80210235C>T , CM000679.2:g.80210235C>T	GRCh38
NC_000017.10:g.78184034C>T , CM000679.1:g.78184034C>T	GRCh37
NC_000017.9:g.75798629C>T	NCBI36
NG_008229.1:g.15166G>A
NG_032778.1:g.45244C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703570.1:n.2844+977C>T (CARD14)
ENST00000326317.11:c.*217G>A (SGSH) MANE Select	ENSP00000314606.6:n.*217G>A
ENST00000326317.10:c.*217G>A (SGSH)	ENSP00000314606.6:n.*217G>A
ENST00000572257.5:c.551+1836G>A (SGSH)
ENST00000573150.5:c.*936G>A (SGSH)	ENSP00000459280.1:n.*936G>A
ENST00000575282.5:n.4609G>A (SGSH)
NM_000199.3:c.*217G>A (SGSH)	NP_000190.1:n.*217G>A
XM_005257583.3:c.949+1836G>A (SGSH)	XP_005257640.1:n.949+1836G>A
NM_000199.4:c.*217G>A (SGSH)	NP_000190.1:n.*217G>A
NM_001352921.1:c.*813G>A (SGSH)	NP_001339850.1:n.*813G>A
NM_001352922.1:c.*776G>A (SGSH)	NP_001339851.1:n.*776G>A
NR_148201.1:n.1707G>A (SGSH)
XM_005257583.4:c.949+1836G>A (SGSH)	XP_005257640.1:n.949+1836G>A
XM_017024952.1:c.*1630G>A (SGSH)	XP_016880441.1:n.*1630G>A
XR_001752585.1:n.1746G>A (SGSH)
XR_001752586.1:n.969+1836G>A (SGSH)
XR_001752587.1:n.969+1836G>A (SGSH)
XR_001752588.1:n.969+1836G>A (SGSH)
XR_001752589.1:n.969+1836G>A (SGSH)
XR_001752590.1:n.969+1836G>A (SGSH)
XR_001752591.1:n.969+1836G>A (SGSH)
XR_001752592.1:n.969+1836G>A (SGSH)
XR_002958057.1:n.1024+1634G>A (SGSH)
NM_000199.5:c.*217G>A (SGSH) MANE Select	NP_000190.1:n.*217G>A
NM_001352921.2:c.*813G>A (SGSH)	NP_001339850.1:n.*813G>A
NM_001352922.2:c.*776G>A (SGSH)	NP_001339851.1:n.*776G>A
NR_148201.2:n.1640G>A (SGSH)
NM_001352921.3:c.*813G>A (SGSH)	NP_001339850.1:n.*813G>A