Canonical Allele Identifier: CA149778

Gene: MVK

Linked Data

• ClinVar Variation Id: 97566
• ClinVar RCV Id: RCV000083818
• dbSNP Id: rs104895359
• MyVariant Identifiers: chr12:g.110034291G>C (hg19) ; chr12:g.109596486G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109596486G>C , CM000674.2:g.109596486G>C	GRCh38
NC_000012.11:g.110034291G>C , CM000674.1:g.110034291G>C	GRCh37
NC_000012.10:g.108518674G>C	NCBI36
NG_007702.1:g.27792G>C , LRG_156:g.27792G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000539696.6:c.257G>C	ENSP00000439134.1:p.Cys86Ser
ENST00000546277.6:c.1100G>C	ENSP00000438153.2:p.Cys367Ser
ENST00000636529.2:n.739G>C
ENST00000697195.1:c.*864G>C	ENSP00000513181.1:n.*864G>C
ENST00000697196.1:c.*273G>C	ENSP00000513182.1:n.*273G>C
ENST00000697197.1:n.3129G>C
ENST00000697198.1:n.1484G>C
ENST00000228510.8:c.1100G>C MANE Select	ENSP00000228510.3:p.Cys367Ser
ENST00000636529.1:c.725G>C
ENST00000636996.1:c.948G>C
ENST00000228510.7:c.1100G>C	ENSP00000228510.3:p.Cys367Ser
ENST00000392727.7:c.944G>C	ENSP00000376487.3:p.Cys315Ser
ENST00000447878.6:c.*547G>C	ENSP00000415555.2:n.*547G>C
ENST00000537237.5:c.*773G>C	ENSP00000445382.1:n.*773G>C
ENST00000539575.4:c.1100G>C	ENSP00000443551.2:p.Cys367Ser
ENST00000539696.5:c.257G>C	ENSP00000439134.1:p.Cys86Ser
ENST00000540353.1:n.3333G>C
ENST00000625889.2:c.944G>C	ENSP00000486846.1:p.Cys315Ser
ENST00000629016.2:c.*547G>C	ENSP00000486804.1:n.*547G>C
NM_000431.3:c.1100G>C	NP_000422.1:p.Cys367Ser
NM_001114185.2:c.1100G>C	NP_001107657.1:p.Cys367Ser
NM_001301182.1:c.944G>C	NP_001288111.1:p.Cys315Ser
XM_011538372.1:c.1100G>C	XP_011536674.1:p.Cys367Ser
XM_017019313.2:c.944G>C	XP_016874802.1:p.Cys315Ser
XM_017019314.1:c.1100G>C	XP_016874803.1:p.Cys367Ser
NM_000431.4:c.1100G>C MANE Select	NP_000422.1:p.Cys367Ser
NM_001114185.3:c.1100G>C	NP_001107657.1:p.Cys367Ser
NM_001301182.2:c.944G>C	NP_001288111.1:p.Cys315Ser