Canonical Allele Identifier: CA2316683230

Gene: CTDP1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.79753655C= , CM000680.2:g.79753655C=	GRCh38
NC_000018.9:g.77513655C= , CM000680.1:g.77513655C=	GRCh37
NC_000018.8:g.75614643C=	NCBI36
NG_007988.1:g.78855C= , LRG_236:g.78855C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000299543.9:c.1043C=
ENST00000590599.2:n.1825C=
ENST00000613122.5:c.2751C= MANE Select	ENSP00000484525.2:p.Gly917=
ENST00000075430.11:c.2588C=	ENSP00000075430.7:p.Ala863=
ENST00000299543.8:c.2394C=	ENSP00000299543.8:p.Gly798=
ENST00000590599.1:n.916C=
ENST00000591598.5:c.2380C=	ENSP00000465119.1:p.Pro794=
ENST00000613122.4:c.2751C=	ENSP00000484525.1:p.Gly917=
NM_001202504.1:c.2394C=	NP_001189433.1:p.Gly798=
NM_004715.4:c.2751C= , LRG_236t1:c.2751C=	NP_004706.3:p.Gly917=
NM_048368.3:c.2588C=	NP_430255.2:p.Ala863=
XM_005266782.2:c.2584C=	XP_005266839.1:p.Pro862=
XM_011526261.1:c.2421C=	XP_011524563.1:p.Gly807=
NM_001318511.1:c.2584C=	NP_001305440.1:p.Pro862=
XM_017026078.1:c.2196C=	XP_016881567.1:p.Gly732=
NM_001318511.2:c.2584C=	NP_001305440.1:p.Pro862=
NM_004715.5:c.2751C= MANE Select	NP_004706.3:p.Gly917=
NM_048368.4:c.2588C=	NP_430255.2:p.Ala863=