Canonical Allele Identifier: CA2316683219
Gene: CTDP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.79753631A= , CM000680.2:g.79753631A= GRCh38
NC_000018.9:g.77513631A= , CM000680.1:g.77513631A= GRCh37
NC_000018.8:g.75614619A= NCBI36
NG_007988.1:g.78831A= , LRG_236:g.78831A=

Transcript Alleles

HGVS Amino-acid change
ENST00000299543.9:c.1040-21A=
ENST00000590599.2:n.1822-21A=
ENST00000613122.5:c.2748-21A= MANE Select ENSP00000484525.2:n.2748-21A=
ENST00000075430.11:c.2585-21A= ENSP00000075430.7:n.2585-21A=
ENST00000299543.8:c.2391-21A= ENSP00000299543.8:n.2391-21A=
ENST00000590599.1:n.913-21A=
ENST00000591598.5:c.2377-21A= ENSP00000465119.1:n.2377-21A=
ENST00000613122.4:c.2748-21A= ENSP00000484525.1:n.2748-21A=
NM_001202504.1:c.2391-21A= NP_001189433.1:n.2391-21A=
NM_004715.4:c.2748-21A= , LRG_236t1:c.2748-21A= NP_004706.3:n.2748-21A=
NM_048368.3:c.2585-21A= NP_430255.2:n.2585-21A=
XM_005266782.2:c.2581-21A= XP_005266839.1:n.2581-21A=
XM_011526261.1:c.2418-21A= XP_011524563.1:n.2418-21A=
NM_001318511.1:c.2581-21A= NP_001305440.1:n.2581-21A=
XM_017026078.1:c.2193-21A= XP_016881567.1:n.2193-21A=
NM_001318511.2:c.2581-21A= NP_001305440.1:n.2581-21A=
NM_004715.5:c.2748-21A= MANE Select NP_004706.3:n.2748-21A=
NM_048368.4:c.2585-21A= NP_430255.2:n.2585-21A=