Canonical Allele Identifier: CA354929309

Gene: CP

Linked Data

• gnomAD v4: 3-149177937-A-G
• MyVariant Identifiers: chr3:g.148895724A>G (hg19) ; chr3:g.149177937A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149177937A>G , CM000665.2:g.149177937A>G	GRCh38
NC_000003.11:g.148895724A>G , CM000665.1:g.148895724A>G	GRCh37
NC_000003.10:g.150378414A>G	NCBI36
NG_011800.1:g.49109T>C
NG_011800.2:g.49109T>C
NG_011800.3:g.49109T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.2921T>C MANE Select	ENSP00000264613.6:p.Met974Thr
ENST00000264613.10:c.2921T>C	ENSP00000264613.6:p.Met974Thr
ENST00000460674.5:n.838T>C
ENST00000463556.5:n.443T>C
ENST00000479771.5:c.326T>C	ENSP00000420367.1:p.Met109Thr
ENST00000481169.5:c.2708T>C	ENSP00000418773.1:p.Met903Thr
ENST00000490639.5:n.2953T>C
ENST00000494544.1:c.2270T>C	ENSP00000420545.1:p.Met757Thr
NM_000096.3:c.2921T>C	NP_000087.1:p.Met974Thr
NR_046371.1:n.2961T>C
XM_006713499.2:c.2921T>C	XP_006713562.1:p.Met974Thr
XM_006713500.2:c.2921T>C	XP_006713563.1:p.Met974Thr
XM_006713501.2:c.2921T>C	XP_006713564.1:p.Met974Thr
XM_011512435.1:c.2921T>C	XP_011510737.1:p.Met974Thr
XR_427361.2:n.3179T>C
XM_006713499.3:c.2921T>C	XP_006713562.1:p.Met974Thr
XM_006713500.4:c.2921T>C	XP_006713563.1:p.Met974Thr
XM_006713501.3:c.2921T>C	XP_006713564.1:p.Met974Thr
XM_011512435.2:c.2921T>C	XP_011510737.1:p.Met974Thr
XM_017005734.2:c.2921T>C	XP_016861223.1:p.Met974Thr
XM_017005735.2:c.2921T>C	XP_016861224.1:p.Met974Thr
XR_427361.3:n.3137T>C
NM_000096.4:c.2921T>C MANE Select	NP_000087.2:p.Met974Thr
NR_046371.2:n.2745T>C