Canonical Allele Identifier: CA454879342

Gene: CCM2

Linked Data

• dbSNP Id: rs1212867410
• gnomAD v2: 7-45077944-T-C
• gnomAD v3: 7-45038345-T-C
• gnomAD v4: 7-45038345-T-C
• MyVariant Identifiers: chr7:g.45077944T>C (hg19) ; chr7:g.45038345T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.45038345T>C , CM000669.2:g.45038345T>C	GRCh38
NC_000007.13:g.45077944T>C , CM000669.1:g.45077944T>C	GRCh37
NC_000007.12:g.45044469T>C	NCBI36
NG_016295.1:g.43158T>C , LRG_664:g.43158T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000258781.11:c.123T>C MANE Select	ENSP00000258781.7:p.Pro41=
ENST00000648329.1:c.123T>C	ENSP00000496916.1:p.Pro41=
ENST00000258781.10:c.123T>C	ENSP00000258781.6:p.Pro41=
ENST00000381112.7:c.186T>C	ENSP00000370503.3:p.Pro62=
ENST00000461377.5:n.476T>C
ENST00000472223.5:n.190T>C
ENST00000474617.1:c.105T>C	ENSP00000419474.1:p.Pro35=
ENST00000475551.5:c.105T>C	ENSP00000417180.1:p.Pro35=
ENST00000476594.1:n.85T>C
ENST00000478169.5:n.345T>C
ENST00000478582.5:n.334T>C
ENST00000480658.5:n.219T>C
ENST00000482714.5:n.126+10548T>C
ENST00000488727.5:c.123T>C	ENSP00000417251.1:p.Pro41=
ENST00000492883.5:n.219T>C
ENST00000541586.5:c.31-25573T>C	ENSP00000444725.1:n.31-25573T>C
ENST00000544363.5:c.123T>C	ENSP00000438035.1:p.Pro41=
NM_001029835.2:c.186T>C , LRG_664t1:c.186T>C	NP_001025006.1:p.Pro62=
NM_001167934.1:c.31-25573T>C	NP_001161406.1:n.31-25573T>C
NM_001167935.1:c.123T>C	NP_001161407.1:p.Pro41=
NM_031443.3:c.123T>C , LRG_664t2:c.123T>C	NP_113631.1:p.Pro41=
NR_030770.1:n.205T>C
XM_006715785.2:c.93+10548T>C	XP_006715848.1:n.93+10548T>C
XM_006715786.2:c.186T>C	XP_006715849.1:p.Pro62=
XM_011515561.1:c.186T>C	XP_011513863.1:p.Pro62=
XM_011515562.1:c.123T>C	XP_011513864.1:p.Pro41=
XM_011515563.1:c.93+10548T>C	XP_011513865.1:n.93+10548T>C
XM_011515564.1:c.31-25573T>C	XP_011513866.1:n.31-25573T>C
XR_428088.2:n.199T>C
NM_001363458.1:c.123T>C	NP_001350387.1:p.Pro41=
NM_001363459.1:c.31-25573T>C	NP_001350388.1:n.31-25573T>C
XM_006715785.4:c.93+10548T>C	XP_006715848.1:n.93+10548T>C
XM_006715786.3:c.186T>C	XP_006715849.1:p.Pro62=
XM_011515561.2:c.186T>C	XP_011513863.1:p.Pro62=
XM_011515563.3:c.93+10548T>C	XP_011513865.1:n.93+10548T>C
XM_017012671.1:c.186T>C	XP_016868160.1:p.Pro62=
XM_017012672.2:c.93+10548T>C	XP_016868161.1:n.93+10548T>C
XM_017012673.1:c.31-25573T>C	XP_016868162.1:n.31-25573T>C
XR_428088.3:n.219T>C
NM_001363458.2:c.123T>C	NP_001350387.1:p.Pro41=
NM_001363459.2:c.31-25573T>C	NP_001350388.1:n.31-25573T>C
NM_031443.4:c.123T>C MANE Select	NP_113631.1:p.Pro41=
NR_030770.2:n.205T>C
NM_001167934.2:c.31-25573T>C	NP_001161406.1:n.31-25573T>C
NM_001167935.2:c.123T>C	NP_001161407.1:p.Pro41=