Canonical Allele Identifier: CA454934969

Gene: DDC FIGNL1

Linked Data

• MyVariant Identifiers: chr7:g.50563068A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.50495370A>G , CM000669.2:g.50495370A>G	GRCh38
NC_000007.13:g.50563068A>G , CM000669.1:g.50563068A>G	GRCh37
NC_000007.12:g.50530562A>G	NCBI36
NG_008742.1:g.75087T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000444124.7:c.924T>C (DDC) MANE Select	ENSP00000403644.2:p.Asn308=
ENST00000357936.9:c.924T>C (DDC)	ENSP00000350616.5:p.Asn308=
ENST00000380984.4:c.924T>C (DDC)	ENSP00000370371.4:p.Asn308=
ENST00000426377.5:c.690T>C (DDC)	ENSP00000395069.1:p.Asn230=
ENST00000430300.5:c.566T>C (DDC)
ENST00000431062.5:c.645T>C (DDC)	ENSP00000399184.1:p.Asn215=
ENST00000444124.6:c.924T>C (DDC)	ENSP00000403644.2:p.Asn308=
ENST00000444733.5:c.*25T>C (DDC)	ENSP00000393724.1:n.*25T>C
ENST00000613602.3:c.-11+47148T>C (FIGNL1)	ENSP00000481751.1:n.-11+47148T>C
ENST00000615193.4:c.645T>C (DDC)	ENSP00000484104.1:p.Asn215=
ENST00000617822.4:c.780T>C (DDC)	ENSP00000478385.1:p.Asn260=
ENST00000622873.4:c.810T>C (DDC)	ENSP00000479110.1:p.Asn270=
NM_000790.3:c.924T>C (DDC)	NP_000781.1:p.Asn308=
NM_001082971.1:c.924T>C (DDC)	NP_001076440.1:p.Asn308=
NM_001242886.1:c.810T>C (DDC)	NP_001229815.1:p.Asn270=
NM_001242887.1:c.780T>C (DDC)	NP_001229816.1:p.Asn260=
NM_001242888.1:c.690T>C (DDC)	NP_001229817.1:p.Asn230=
NM_001242889.1:c.645T>C (DDC)	NP_001229818.1:p.Asn215=
NM_001242890.1:c.924T>C (DDC)	NP_001229819.1:p.Asn308=
XM_005271745.3:c.810T>C (DDC)	XP_005271802.1:p.Asn270=
XM_011515161.1:c.573T>C (DDC)	XP_011513463.1:p.Asn191=
XM_005271745.4:c.810T>C (DDC)	XP_005271802.1:p.Asn270=
XM_011515161.2:c.867T>C (DDC)	XP_011513463.2:p.Asn289=
NM_001082971.2:c.924T>C (DDC) MANE Select	NP_001076440.2:p.Asn308=
NM_000790.4:c.924T>C (DDC)	NP_000781.2:p.Asn308=
NM_001242888.2:c.690T>C (DDC)	NP_001229817.2:p.Asn230=
NM_001242890.2:c.924T>C (DDC)	NP_001229819.2:p.Asn308=
NM_001242886.2:c.810T>C (DDC)	NP_001229815.2:p.Asn270=
NM_001242887.2:c.780T>C (DDC)	NP_001229816.2:p.Asn260=
NM_001242889.2:c.645T>C (DDC)	NP_001229818.2:p.Asn215=