Canonical Allele Identifier: CA844720182

Gene: NCALD

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.101932635G>C , CM000670.2:g.101932635G>C	GRCh38
NC_000008.10:g.102944863G>C , CM000670.1:g.102944863G>C	GRCh37
NC_000008.9:g.103014039G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311028.4:c.-156-16777C>G	ENSP00000310587.3:n.-156-16777C>G
ENST00000395923.5:c.-69-16777C>G	ENSP00000379256.1:n.-69-16777C>G
ENST00000517531.5:c.-69-16777C>G	ENSP00000429245.1:n.-69-16777C>G
ENST00000517639.5:n.79-16777C>G
ENST00000517822.5:c.-168-16777C>G	ENSP00000428312.1:n.-168-16777C>G
ENST00000518166.5:c.-69-16777C>G	ENSP00000429522.1:n.-69-16777C>G
ENST00000518661.5:c.-156-16777C>G	ENSP00000428093.1:n.-156-16777C>G
ENST00000518727.5:c.-69-16777C>G	ENSP00000430731.1:n.-69-16777C>G
ENST00000518952.5:n.79-16777C>G
ENST00000520425.5:c.-69-16777C>G	ENSP00000430925.1:n.-69-16777C>G
ENST00000520690.5:c.-69-16777C>G	ENSP00000429255.1:n.-69-16777C>G
ENST00000521599.5:c.-69-16777C>G	ENSP00000428105.1:n.-69-16777C>G
ENST00000521964.5:c.-156-16777C>G	ENSP00000430064.1:n.-156-16777C>G
ENST00000522078.5:c.-156-16777C>G	ENSP00000429162.1:n.-156-16777C>G
ENST00000522206.5:c.-69-16777C>G	ENSP00000429296.1:n.-69-16777C>G
ENST00000523923.5:c.-224-16777C>G	ENSP00000428193.1:n.-224-16777C>G
ENST00000524209.5:c.-159-16777C>G	ENSP00000429493.1:n.-159-16777C>G
NM_001040624.1:c.-156-16777C>G	NP_001035714.1:n.-156-16777C>G
NM_001040625.1:c.-69-16777C>G	NP_001035715.1:n.-69-16777C>G
NM_001040626.1:c.-156-16777C>G	NP_001035716.1:n.-156-16777C>G
NM_001040627.1:c.-69-16777C>G	NP_001035717.1:n.-69-16777C>G
NM_001040628.1:c.-125-16777C>G	NP_001035718.1:n.-125-16777C>G
NM_001040629.1:c.-125-16777C>G	NP_001035719.1:n.-125-16777C>G
NM_001040630.1:c.-69-16777C>G	NP_001035720.1:n.-69-16777C>G
XM_011517333.1:c.-224-16777C>G	XP_011515635.1:n.-224-16777C>G
XM_011517333.2:c.-224-16777C>G	XP_011515635.1:n.-224-16777C>G
XM_017013900.1:c.374-16777C>G	XP_016869389.1:n.374-16777C>G
XM_017013901.1:c.-156-16777C>G	XP_016869390.1:n.-156-16777C>G
XM_024447296.1:c.-69-16777C>G	XP_024303064.1:n.-69-16777C>G
XM_024447297.1:c.-156-16777C>G	XP_024303065.1:n.-156-16777C>G
XM_024447298.1:c.-232-16777C>G	XP_024303066.1:n.-232-16777C>G
XM_024447299.1:c.-168-16777C>G	XP_024303067.1:n.-168-16777C>G
XM_024447300.1:c.-159-16777C>G	XP_024303068.1:n.-159-16777C>G
XM_024447301.1:c.-232-16777C>G	XP_024303069.1:n.-232-16777C>G
XM_024447302.1:c.-69-16777C>G	XP_024303070.1:n.-69-16777C>G
XR_001745607.1:n.468-16777C>G
NM_001040624.2:c.-156-16777C>G	NP_001035714.1:n.-156-16777C>G
NM_001040625.2:c.-69-16777C>G	NP_001035715.1:n.-69-16777C>G
NM_001040626.2:c.-156-16777C>G	NP_001035716.1:n.-156-16777C>G
NM_001040627.2:c.-69-16777C>G	NP_001035717.1:n.-69-16777C>G
NM_001040628.2:c.-125-16777C>G	NP_001035718.1:n.-125-16777C>G
NM_001040629.2:c.-125-16777C>G	NP_001035719.1:n.-125-16777C>G
NM_001040630.2:c.-69-16777C>G	NP_001035720.1:n.-69-16777C>G