Canonical Allele Identifier: CA502404750

Gene: CARD14 SGSH

Linked Data

• MyVariant Identifiers: chr17:g.78185931C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80212132C>G , CM000679.2:g.80212132C>G	GRCh38
NC_000017.10:g.78185931C>G , CM000679.1:g.78185931C>G	GRCh37
NC_000017.9:g.75800526C>G	NCBI36
NG_008229.1:g.13269G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000703570.1:n.2844+2874C>G (CARD14)
ENST00000326317.11:c.888G>C (SGSH) MANE Select	ENSP00000314606.6:p.Val296=
ENST00000326317.10:c.888G>C (SGSH)	ENSP00000314606.6:p.Val296=
ENST00000570923.1:c.*98G>C (SGSH)	ENSP00000458200.1:n.*98G>C
ENST00000572257.5:c.490G>C (SGSH)
ENST00000573150.5:c.*98G>C (SGSH)	ENSP00000459280.1:n.*98G>C
ENST00000575282.5:n.2712G>C (SGSH)
ENST00000576856.1:c.87G>C (SGSH)	ENSP00000460720.1:p.Val29=
NM_000199.3:c.888G>C (SGSH)	NP_000190.1:p.Val296=
XM_005257582.2:c.888G>C (SGSH)	XP_005257639.1:p.Val296=
XM_005257583.3:c.888G>C (SGSH)	XP_005257640.1:p.Val296=
XM_011525126.1:c.888G>C (SGSH)	XP_011523428.1:p.Val296=
XM_011525127.1:c.888G>C (SGSH)	XP_011523429.1:p.Val296=
XR_934532.1:n.908G>C (SGSH)
NM_000199.4:c.888G>C (SGSH)	NP_000190.1:p.Val296=
NM_001352921.1:c.888G>C (SGSH)	NP_001339850.1:p.Val296=
NM_001352922.1:c.888G>C (SGSH)	NP_001339851.1:p.Val296=
NR_148201.1:n.869G>C (SGSH)
XM_005257583.4:c.888G>C (SGSH)	XP_005257640.1:p.Val296=
XM_017024952.1:c.888G>C (SGSH)	XP_016880441.1:p.Val296=
XR_001752585.1:n.908G>C (SGSH)
XR_001752586.1:n.908G>C (SGSH)
XR_001752587.1:n.908G>C (SGSH)
XR_001752588.1:n.908G>C (SGSH)
XR_001752589.1:n.908G>C (SGSH)
XR_001752590.1:n.908G>C (SGSH)
XR_001752591.1:n.908G>C (SGSH)
XR_001752592.1:n.908G>C (SGSH)
XR_002958057.1:n.908G>C (SGSH)
XR_934532.2:n.908G>C (SGSH)
NM_000199.5:c.888G>C (SGSH) MANE Select	NP_000190.1:p.Val296=
NM_001352921.2:c.888G>C (SGSH)	NP_001339850.1:p.Val296=
NM_001352922.2:c.888G>C (SGSH)	NP_001339851.1:p.Val296=
NR_148201.2:n.802G>C (SGSH)
NM_001352921.3:c.888G>C (SGSH)	NP_001339850.1:p.Val296=