Canonical Allele Identifier: CA367538077

Gene: DDC FIGNL1

Linked Data

• MyVariant Identifiers: chr7:g.50563072A>G (hg19) ; chr7:g.50495374A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.50495374A>G , CM000669.2:g.50495374A>G	GRCh38
NC_000007.13:g.50563072A>G , CM000669.1:g.50563072A>G	GRCh37
NC_000007.12:g.50530566A>G	NCBI36
NG_008742.1:g.75083T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000444124.7:c.920T>C (DDC) MANE Select	ENSP00000403644.2:p.Val307Ala
ENST00000357936.9:c.920T>C (DDC)	ENSP00000350616.5:p.Val307Ala
ENST00000380984.4:c.920T>C (DDC)	ENSP00000370371.4:p.Val307Ala
ENST00000426377.5:c.686T>C (DDC)	ENSP00000395069.1:p.Val229Ala
ENST00000430300.5:c.562T>C (DDC)
ENST00000431062.5:c.641T>C (DDC)	ENSP00000399184.1:p.Val214Ala
ENST00000444124.6:c.920T>C (DDC)	ENSP00000403644.2:p.Val307Ala
ENST00000444733.5:c.*21T>C (DDC)	ENSP00000393724.1:n.*21T>C
ENST00000613602.3:c.-11+47144T>C (FIGNL1)	ENSP00000481751.1:n.-11+47144T>C
ENST00000615193.4:c.641T>C (DDC)	ENSP00000484104.1:p.Val214Ala
ENST00000617822.4:c.776T>C (DDC)	ENSP00000478385.1:p.Val259Ala
ENST00000622873.4:c.806T>C (DDC)	ENSP00000479110.1:p.Val269Ala
NM_000790.3:c.920T>C (DDC)	NP_000781.1:p.Val307Ala
NM_001082971.1:c.920T>C (DDC)	NP_001076440.1:p.Val307Ala
NM_001242886.1:c.806T>C (DDC)	NP_001229815.1:p.Val269Ala
NM_001242887.1:c.776T>C (DDC)	NP_001229816.1:p.Val259Ala
NM_001242888.1:c.686T>C (DDC)	NP_001229817.1:p.Val229Ala
NM_001242889.1:c.641T>C (DDC)	NP_001229818.1:p.Val214Ala
NM_001242890.1:c.920T>C (DDC)	NP_001229819.1:p.Val307Ala
XM_005271745.3:c.806T>C (DDC)	XP_005271802.1:p.Val269Ala
XM_011515161.1:c.569T>C (DDC)	XP_011513463.1:p.Val190Ala
XM_005271745.4:c.806T>C (DDC)	XP_005271802.1:p.Val269Ala
XM_011515161.2:c.863T>C (DDC)	XP_011513463.2:p.Val288Ala
NM_001082971.2:c.920T>C (DDC) MANE Select	NP_001076440.2:p.Val307Ala
NM_000790.4:c.920T>C (DDC)	NP_000781.2:p.Val307Ala
NM_001242888.2:c.686T>C (DDC)	NP_001229817.2:p.Val229Ala
NM_001242890.2:c.920T>C (DDC)	NP_001229819.2:p.Val307Ala
NM_001242886.2:c.806T>C (DDC)	NP_001229815.2:p.Val269Ala
NM_001242887.2:c.776T>C (DDC)	NP_001229816.2:p.Val259Ala
NM_001242889.2:c.641T>C (DDC)	NP_001229818.2:p.Val214Ala