Canonical Allele Identifier: CA627804999

Gene: CSNK1D

Linked Data

• dbSNP Id: rs1187503032
• gnomAD v2: 17-80223683-AAAG-A
• gnomAD v4: 17-82265807-AAAG-A
• MyVariant Identifiers: chr17:g.80223684_80223686del (hg19) ; chr17:g.82265808_82265810del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82265810_82265812del , CM000679.2:g.82265810_82265812del	GRCh38
NC_000017.10:g.80223686_80223688del , CM000679.1:g.80223686_80223688del	GRCh37
NC_000017.9:g.77816975_77816977del	NCBI36
NG_012828.1:g.12888_12890del
NG_012828.2:g.12933_12935del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392334.7:c.77-14_77-12del	ENSP00000376146.2:n.77-14_77-12del
ENST00000314028.11:c.77-14_77-12del MANE Select	ENSP00000324464.6:n.77-14_77-12del
ENST00000314028.10:c.77-14_77-12del	ENSP00000324464.6:n.77-14_77-12del
ENST00000392334.6:c.77-14_77-12del	ENSP00000376146.2:n.77-14_77-12del
ENST00000398519.9:c.77-14_77-12del	ENSP00000381531.5:n.77-14_77-12del
ENST00000403276.7:c.77-14_77-12del	ENSP00000385769.3:n.77-14_77-12del
ENST00000578194.5:n.283-14_283-12del
ENST00000579308.1:n.102-14_102-12del
ENST00000579316.5:n.134-14_134-12del
ENST00000580061.5:n.77-14_77-12del
ENST00000580446.1:c.76+7496_76+7498del	ENSP00000463757.1:n.76+7496_76+7498del
ENST00000581241.5:n.65-14_65-12del
ENST00000581660.5:c.*115-14_*115-12del	ENSP00000464551.1:n.*115-14_*115-12del
ENST00000582844.5:n.35-14_35-12del
ENST00000584472.5:n.162-14_162-12del
ENST00000585026.1:c.*123-14_*123-12del	ENSP00000462144.1:n.*123-14_*123-12del
NM_001893.4:c.77-14_77-12del	NP_001884.2:n.77-14_77-12del
NM_139062.2:c.77-14_77-12del	NP_620693.1:n.77-14_77-12del
NR_110578.1:n.438-14_438-12del
XM_005256336.2:c.77-14_77-12del	XP_005256393.1:n.77-14_77-12del
XM_005256337.3:c.77-14_77-12del	XP_005256394.1:n.77-14_77-12del
XR_243518.2:n.397-14_397-12del
XR_430028.2:n.397-14_397-12del
XR_933922.1:n.397-14_397-12del
XR_933923.1:n.397-14_397-12del
NM_001363749.1:c.77-14_77-12del	NP_001350678.1:n.77-14_77-12del
NM_001893.5:c.77-14_77-12del	NP_001884.2:n.77-14_77-12del
NM_139062.3:c.77-14_77-12del	NP_620693.1:n.77-14_77-12del
NR_110578.2:n.446-14_446-12del
XM_005256336.4:c.77-14_77-12del	XP_005256393.1:n.77-14_77-12del
XR_002957961.1:n.396-14_396-12del
XR_243518.4:n.396-14_396-12del
XR_430028.4:n.396-14_396-12del
XR_933922.3:n.396-14_396-12del
XR_933923.3:n.396-14_396-12del
NM_001363749.2:c.77-14_77-12del	NP_001350678.1:n.77-14_77-12del
NM_001893.6:c.77-14_77-12del MANE Select	NP_001884.2:n.77-14_77-12del
NM_139062.4:c.77-14_77-12del	NP_620693.1:n.77-14_77-12del