Canonical Allele Identifier: CA10629245

Gene: DDC FIGNL1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.50458565A>G , CM000669.2:g.50458565A>G	GRCh38
NC_000007.13:g.50526263A>G , CM000669.1:g.50526263A>G	GRCh37
NC_000007.12:g.50493757A>G	NCBI36
NG_008742.1:g.111892T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001082971.2:c.*297T>C (DDC) MANE Select	NP_001076440.2:n.*297T>C
ENST00000444124.7:c.*297T>C (DDC) MANE Select	ENSP00000403644.2:n.*297T>C
NM_000790.3:c.*297T>C (DDC)	NP_000781.1:n.*297T>C
NM_000790.4:c.*297T>C (DDC)	NP_000781.2:n.*297T>C
NM_001082971.1:c.*297T>C (DDC)	NP_001076440.1:n.*297T>C
NM_001242886.1:c.*297T>C (DDC)	NP_001229815.1:n.*297T>C
NM_001242886.2:c.*297T>C (DDC)	NP_001229815.2:n.*297T>C
NM_001242887.1:c.*297T>C (DDC)	NP_001229816.1:n.*297T>C
NM_001242887.2:c.*297T>C (DDC)	NP_001229816.2:n.*297T>C
NM_001242888.1:c.*297T>C (DDC)	NP_001229817.1:n.*297T>C
NM_001242888.2:c.*297T>C (DDC)	NP_001229817.2:n.*297T>C
NM_001242889.1:c.*297T>C (DDC)	NP_001229818.1:n.*297T>C
NM_001242889.2:c.*297T>C (DDC)	NP_001229818.2:n.*297T>C
ENST00000357936.9:c.*297T>C (DDC)	ENSP00000350616.5:n.*297T>C
ENST00000426377.5:c.*297T>C (DDC)	ENSP00000395069.1:n.*297T>C
ENST00000430300.5:c.1382T>C (DDC)
ENST00000431062.5:c.*297T>C (DDC)	ENSP00000399184.1:n.*297T>C
ENST00000444124.6:c.*297T>C (DDC)	ENSP00000403644.2:n.*297T>C
ENST00000444733.5:c.*841T>C (DDC)	ENSP00000393724.1:n.*841T>C
ENST00000495320.1:n.324T>C (DDC)
ENST00000613602.3:c.-10-11268T>C (FIGNL1)	ENSP00000481751.1:n.-10-11268T>C
ENST00000615193.4:c.*297T>C (DDC)	ENSP00000484104.1:n.*297T>C
ENST00000617822.4:c.*297T>C (DDC)	ENSP00000478385.1:n.*297T>C
ENST00000622873.4:c.*297T>C (DDC)	ENSP00000479110.1:n.*297T>C
XM_005271745.3:c.*297T>C (DDC)	XP_005271802.1:n.*297T>C
XM_005271745.4:c.*297T>C (DDC)	XP_005271802.1:n.*297T>C
XM_011515161.1:c.*297T>C (DDC)	XP_011513463.1:n.*297T>C
XM_011515161.2:c.*297T>C (DDC)	XP_011513463.2:n.*297T>C