Canonical Allele Identifier: CA402835591

Gene: CTDP1

Linked Data

• dbSNP Id: rs2087044737
• MyVariant Identifiers: chr18:g.77513654G>A (hg19) ; chr18:g.79753654G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.79753654G>A , CM000680.2:g.79753654G>A	GRCh38
NC_000018.9:g.77513654G>A , CM000680.1:g.77513654G>A	GRCh37
NC_000018.8:g.75614642G>A	NCBI36
NG_007988.1:g.78854G>A , LRG_236:g.78854G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000299543.9:c.1042G>A
ENST00000590599.2:n.1824G>A
ENST00000613122.5:c.2750G>A MANE Select	ENSP00000484525.2:p.Gly917Asp
ENST00000075430.11:c.2587G>A	ENSP00000075430.7:p.Ala863Thr
ENST00000299543.8:c.2393G>A	ENSP00000299543.8:p.Gly798Asp
ENST00000590599.1:n.915G>A
ENST00000591598.5:c.2379G>A	ENSP00000465119.1:p.Arg793=
ENST00000613122.4:c.2750G>A	ENSP00000484525.1:p.Gly917Asp
NM_001202504.1:c.2393G>A	NP_001189433.1:p.Gly798Asp
NM_004715.4:c.2750G>A , LRG_236t1:c.2750G>A	NP_004706.3:p.Gly917Asp
NM_048368.3:c.2587G>A	NP_430255.2:p.Ala863Thr
XM_005266782.2:c.2583G>A	XP_005266839.1:p.Arg861=
XM_011526261.1:c.2420G>A	XP_011524563.1:p.Gly807Asp
NM_001318511.1:c.2583G>A	NP_001305440.1:p.Arg861=
XM_017026078.1:c.2195G>A	XP_016881567.1:p.Gly732Asp
NM_001318511.2:c.2583G>A	NP_001305440.1:p.Arg861=
NM_004715.5:c.2750G>A MANE Select	NP_004706.3:p.Gly917Asp
NM_048368.4:c.2587G>A	NP_430255.2:p.Ala863Thr