Canonical Allele Identifier: CA436213060

Gene: CP

Linked Data

• MyVariant Identifiers: chr3:g.148895630G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149177843G>A , CM000665.2:g.149177843G>A	GRCh38
NC_000003.11:g.148895630G>A , CM000665.1:g.148895630G>A	GRCh37
NC_000003.10:g.150378320G>A	NCBI36
NG_011800.1:g.49203C>T
NG_011800.2:g.49203C>T
NG_011800.3:g.49203C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.3015C>T MANE Select	ENSP00000264613.6:p.Tyr1005=
ENST00000264613.10:c.3015C>T	ENSP00000264613.6:p.Tyr1005=
ENST00000460674.5:n.932C>T
ENST00000463556.5:n.537C>T
ENST00000473296.1:n.65C>T
ENST00000479771.5:c.420C>T	ENSP00000420367.1:p.Tyr140=
ENST00000481169.5:c.2802C>T	ENSP00000418773.1:p.Tyr934=
ENST00000490639.5:n.3047C>T
ENST00000494544.1:c.2364C>T	ENSP00000420545.1:p.Tyr788=
NM_000096.3:c.3015C>T	NP_000087.1:p.Tyr1005=
NR_046371.1:n.3055C>T
XM_006713499.2:c.3015C>T	XP_006713562.1:p.Tyr1005=
XM_006713500.2:c.3015C>T	XP_006713563.1:p.Tyr1005=
XM_006713501.2:c.3015C>T	XP_006713564.1:p.Tyr1005=
XM_011512435.1:c.3015C>T	XP_011510737.1:p.Tyr1005=
XR_427361.2:n.3273C>T
XM_006713499.3:c.3015C>T	XP_006713562.1:p.Tyr1005=
XM_006713500.4:c.3015C>T	XP_006713563.1:p.Tyr1005=
XM_006713501.3:c.3015C>T	XP_006713564.1:p.Tyr1005=
XM_011512435.2:c.3015C>T	XP_011510737.1:p.Tyr1005=
XM_017005734.2:c.3015C>T	XP_016861223.1:p.Tyr1005=
XM_017005735.2:c.3015C>T	XP_016861224.1:p.Tyr1005=
XR_427361.3:n.3231C>T
NM_000096.4:c.3015C>T MANE Select	NP_000087.2:p.Tyr1005=
NR_046371.2:n.2839C>T