Canonical Allele Identifier: CA354929218

Gene: CP

Linked Data

• MyVariant Identifiers: chr3:g.148895686T>G (hg19) ; chr3:g.149177899T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149177899T>G , CM000665.2:g.149177899T>G	GRCh38
NC_000003.11:g.148895686T>G , CM000665.1:g.148895686T>G	GRCh37
NC_000003.10:g.150378376T>G	NCBI36
NG_011800.1:g.49147A>C
NG_011800.2:g.49147A>C
NG_011800.3:g.49147A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.2959A>C MANE Select	ENSP00000264613.6:p.Met987Leu
ENST00000264613.10:c.2959A>C	ENSP00000264613.6:p.Met987Leu
ENST00000460674.5:n.876A>C
ENST00000463556.5:n.481A>C
ENST00000473296.1:n.9A>C
ENST00000479771.5:c.364A>C	ENSP00000420367.1:p.Met122Leu
ENST00000481169.5:c.2746A>C	ENSP00000418773.1:p.Met916Leu
ENST00000490639.5:n.2991A>C
ENST00000494544.1:c.2308A>C	ENSP00000420545.1:p.Met770Leu
NM_000096.3:c.2959A>C	NP_000087.1:p.Met987Leu
NR_046371.1:n.2999A>C
XM_006713499.2:c.2959A>C	XP_006713562.1:p.Met987Leu
XM_006713500.2:c.2959A>C	XP_006713563.1:p.Met987Leu
XM_006713501.2:c.2959A>C	XP_006713564.1:p.Met987Leu
XM_011512435.1:c.2959A>C	XP_011510737.1:p.Met987Leu
XR_427361.2:n.3217A>C
XM_006713499.3:c.2959A>C	XP_006713562.1:p.Met987Leu
XM_006713500.4:c.2959A>C	XP_006713563.1:p.Met987Leu
XM_006713501.3:c.2959A>C	XP_006713564.1:p.Met987Leu
XM_011512435.2:c.2959A>C	XP_011510737.1:p.Met987Leu
XM_017005734.2:c.2959A>C	XP_016861223.1:p.Met987Leu
XM_017005735.2:c.2959A>C	XP_016861224.1:p.Met987Leu
XR_427361.3:n.3175A>C
NM_000096.4:c.2959A>C MANE Select	NP_000087.2:p.Met987Leu
NR_046371.2:n.2783A>C