Canonical Allele Identifier: CA401363082

Gene: CARD14 SGSH

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80214725G>C , CM000679.2:g.80214725G>C	GRCh38
NC_000017.10:g.78188524G>C , CM000679.1:g.78188524G>C	GRCh37
NC_000017.9:g.75803119G>C	NCBI36
NG_008229.1:g.10676C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000199.5:c.396C>G (SGSH) MANE Select	NP_000190.1:p.Tyr132Ter
ENST00000326317.11:c.396C>G (SGSH) MANE Select	ENSP00000314606.6:p.Tyr132Ter
NM_000199.3:c.396C>G (SGSH)	NP_000190.1:p.Tyr132Ter
NM_000199.4:c.396C>G (SGSH)	NP_000190.1:p.Tyr132Ter
NM_001352921.1:c.396C>G (SGSH)	NP_001339850.1:p.Tyr132Ter
NM_001352921.2:c.396C>G (SGSH)	NP_001339850.1:p.Tyr132Ter
NM_001352921.3:c.396C>G (SGSH)	NP_001339850.1:p.Tyr132Ter
NM_001352922.1:c.396C>G (SGSH)	NP_001339851.1:p.Tyr132Ter
NM_001352922.2:c.396C>G (SGSH)	NP_001339851.1:p.Tyr132Ter
NR_148201.1:n.377C>G (SGSH)
NR_148201.2:n.310C>G (SGSH)
ENST00000326317.10:c.396C>G (SGSH)	ENSP00000314606.6:p.Tyr132Ter
ENST00000570427.1:c.414C>G (SGSH)	ENSP00000459765.1:p.Tyr138Ter
ENST00000570923.1:c.431C>G (SGSH)	ENSP00000458200.1:p.Thr144Ser
ENST00000571051.5:n.375+308C>G (SGSH)
ENST00000571675.5:n.416C>G (SGSH)
ENST00000572208.5:n.373+308C>G (SGSH)
ENST00000573150.5:c.290C>G (SGSH)	ENSP00000459280.1:p.Thr97Ser
ENST00000574505.5:c.301-46C>G (SGSH)
ENST00000575282.5:n.405C>G (SGSH)
ENST00000576707.5:c.135C>G (SGSH)	ENSP00000461128.1:p.Tyr45Ter
ENST00000576941.5:c.250-397C>G (SGSH)	ENSP00000461160.1:n.250-397C>G
ENST00000703570.1:n.2845-1141G>C (CARD14)
XM_005257582.2:c.396C>G (SGSH)	XP_005257639.1:p.Tyr132Ter
XM_005257583.3:c.396C>G (SGSH)	XP_005257640.1:p.Tyr132Ter
XM_005257583.4:c.396C>G (SGSH)	XP_005257640.1:p.Tyr132Ter
XM_011525126.1:c.396C>G (SGSH)	XP_011523428.1:p.Tyr132Ter
XM_011525127.1:c.396C>G (SGSH)	XP_011523429.1:p.Tyr132Ter
XM_017024952.1:c.396C>G (SGSH)	XP_016880441.1:p.Tyr132Ter
XR_001752585.1:n.416C>G (SGSH)
XR_001752586.1:n.416C>G (SGSH)
XR_001752587.1:n.416C>G (SGSH)
XR_001752588.1:n.416C>G (SGSH)
XR_001752589.1:n.416C>G (SGSH)
XR_001752590.1:n.416C>G (SGSH)
XR_001752591.1:n.416C>G (SGSH)
XR_001752592.1:n.416C>G (SGSH)
XR_002958057.1:n.416C>G (SGSH)
XR_934532.1:n.416C>G (SGSH)
XR_934532.2:n.416C>G (SGSH)