Canonical Allele Identifier: CA367531297

Gene: DDC FIGNL1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.50467228A>C , CM000669.2:g.50467228A>C	GRCh38
NC_000007.13:g.50534926A>C , CM000669.1:g.50534926A>C	GRCh37
NC_000007.12:g.50502420A>C	NCBI36
NG_008742.1:g.103229T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001082971.2:c.1228T>G (DDC) MANE Select	NP_001076440.2:p.Cys410Gly
ENST00000444124.7:c.1228T>G (DDC) MANE Select	ENSP00000403644.2:p.Cys410Gly
NM_000790.3:c.1228T>G (DDC)	NP_000781.1:p.Cys410Gly
NM_000790.4:c.1228T>G (DDC)	NP_000781.2:p.Cys410Gly
NM_001082971.1:c.1228T>G (DDC)	NP_001076440.1:p.Cys410Gly
NM_001242886.1:c.1114T>G (DDC)	NP_001229815.1:p.Cys372Gly
NM_001242886.2:c.1114T>G (DDC)	NP_001229815.2:p.Cys372Gly
NM_001242887.1:c.1084T>G (DDC)	NP_001229816.1:p.Cys362Gly
NM_001242887.2:c.1084T>G (DDC)	NP_001229816.2:p.Cys362Gly
NM_001242888.1:c.994T>G (DDC)	NP_001229817.1:p.Cys332Gly
NM_001242888.2:c.994T>G (DDC)	NP_001229817.2:p.Cys332Gly
NM_001242889.1:c.949T>G (DDC)	NP_001229818.1:p.Cys317Gly
NM_001242889.2:c.949T>G (DDC)	NP_001229818.2:p.Cys317Gly
ENST00000357936.9:c.1228T>G (DDC)	ENSP00000350616.5:p.Cys410Gly
ENST00000426377.5:c.994T>G (DDC)	ENSP00000395069.1:p.Cys332Gly
ENST00000430300.5:c.870T>G (DDC)
ENST00000431062.5:c.949T>G (DDC)	ENSP00000399184.1:p.Cys317Gly
ENST00000444124.6:c.1228T>G (DDC)	ENSP00000403644.2:p.Cys410Gly
ENST00000444733.5:c.*329T>G (DDC)	ENSP00000393724.1:n.*329T>G
ENST00000494914.1:n.384T>G (DDC)
ENST00000613602.3:c.-10-19931T>G (FIGNL1)	ENSP00000481751.1:n.-10-19931T>G
ENST00000615193.4:c.949T>G (DDC)	ENSP00000484104.1:p.Cys317Gly
ENST00000617822.4:c.1084T>G (DDC)	ENSP00000478385.1:p.Cys362Gly
ENST00000622873.4:c.1114T>G (DDC)	ENSP00000479110.1:p.Cys372Gly
XM_005271745.3:c.1114T>G (DDC)	XP_005271802.1:p.Cys372Gly
XM_005271745.4:c.1114T>G (DDC)	XP_005271802.1:p.Cys372Gly
XM_011515161.1:c.877T>G (DDC)	XP_011513463.1:p.Cys293Gly
XM_011515161.2:c.1171T>G (DDC)	XP_011513463.2:p.Cys391Gly