Canonical Allele Identifier: CA354929090

Gene: CP

Linked Data

• MyVariant Identifiers: chr3:g.148895631T>A (hg19) ; chr3:g.149177844T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149177844T>A , CM000665.2:g.149177844T>A	GRCh38
NC_000003.11:g.148895631T>A , CM000665.1:g.148895631T>A	GRCh37
NC_000003.10:g.150378321T>A	NCBI36
NG_011800.1:g.49202A>T
NG_011800.2:g.49202A>T
NG_011800.3:g.49202A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.3014A>T MANE Select	ENSP00000264613.6:p.Tyr1005Phe
ENST00000264613.10:c.3014A>T	ENSP00000264613.6:p.Tyr1005Phe
ENST00000460674.5:n.931A>T
ENST00000463556.5:n.536A>T
ENST00000473296.1:n.64A>T
ENST00000479771.5:c.419A>T	ENSP00000420367.1:p.Tyr140Phe
ENST00000481169.5:c.2801A>T	ENSP00000418773.1:p.Tyr934Phe
ENST00000490639.5:n.3046A>T
ENST00000494544.1:c.2363A>T	ENSP00000420545.1:p.Tyr788Phe
NM_000096.3:c.3014A>T	NP_000087.1:p.Tyr1005Phe
NR_046371.1:n.3054A>T
XM_006713499.2:c.3014A>T	XP_006713562.1:p.Tyr1005Phe
XM_006713500.2:c.3014A>T	XP_006713563.1:p.Tyr1005Phe
XM_006713501.2:c.3014A>T	XP_006713564.1:p.Tyr1005Phe
XM_011512435.1:c.3014A>T	XP_011510737.1:p.Tyr1005Phe
XR_427361.2:n.3272A>T
XM_006713499.3:c.3014A>T	XP_006713562.1:p.Tyr1005Phe
XM_006713500.4:c.3014A>T	XP_006713563.1:p.Tyr1005Phe
XM_006713501.3:c.3014A>T	XP_006713564.1:p.Tyr1005Phe
XM_011512435.2:c.3014A>T	XP_011510737.1:p.Tyr1005Phe
XM_017005734.2:c.3014A>T	XP_016861223.1:p.Tyr1005Phe
XM_017005735.2:c.3014A>T	XP_016861224.1:p.Tyr1005Phe
XR_427361.3:n.3230A>T
NM_000096.4:c.3014A>T MANE Select	NP_000087.2:p.Tyr1005Phe
NR_046371.2:n.2838A>T