Canonical Allele Identifier: CA354929279

Gene: CP

Linked Data

• MyVariant Identifiers: chr3:g.148895712T>A (hg19) ; chr3:g.149177925T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149177925T>A , CM000665.2:g.149177925T>A	GRCh38
NC_000003.11:g.148895712T>A , CM000665.1:g.148895712T>A	GRCh37
NC_000003.10:g.150378402T>A	NCBI36
NG_011800.1:g.49121A>T
NG_011800.2:g.49121A>T
NG_011800.3:g.49121A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.2933A>T MANE Select	ENSP00000264613.6:p.Asp978Val
ENST00000264613.10:c.2933A>T	ENSP00000264613.6:p.Asp978Val
ENST00000460674.5:n.850A>T
ENST00000463556.5:n.455A>T
ENST00000479771.5:c.338A>T	ENSP00000420367.1:p.Asp113Val
ENST00000481169.5:c.2720A>T	ENSP00000418773.1:p.Asp907Val
ENST00000490639.5:n.2965A>T
ENST00000494544.1:c.2282A>T	ENSP00000420545.1:p.Asp761Val
NM_000096.3:c.2933A>T	NP_000087.1:p.Asp978Val
NR_046371.1:n.2973A>T
XM_006713499.2:c.2933A>T	XP_006713562.1:p.Asp978Val
XM_006713500.2:c.2933A>T	XP_006713563.1:p.Asp978Val
XM_006713501.2:c.2933A>T	XP_006713564.1:p.Asp978Val
XM_011512435.1:c.2933A>T	XP_011510737.1:p.Asp978Val
XR_427361.2:n.3191A>T
XM_006713499.3:c.2933A>T	XP_006713562.1:p.Asp978Val
XM_006713500.4:c.2933A>T	XP_006713563.1:p.Asp978Val
XM_006713501.3:c.2933A>T	XP_006713564.1:p.Asp978Val
XM_011512435.2:c.2933A>T	XP_011510737.1:p.Asp978Val
XM_017005734.2:c.2933A>T	XP_016861223.1:p.Asp978Val
XM_017005735.2:c.2933A>T	XP_016861224.1:p.Asp978Val
XR_427361.3:n.3149A>T
NM_000096.4:c.2933A>T MANE Select	NP_000087.2:p.Asp978Val
NR_046371.2:n.2757A>T