Canonical Allele Identifier: CA386651298

Gene: MVK

Linked Data

• MyVariant Identifiers: chr12:g.110034273C>G (hg19) ; chr12:g.109596468C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109596468C>G , CM000674.2:g.109596468C>G	GRCh38
NC_000012.11:g.110034273C>G , CM000674.1:g.110034273C>G	GRCh37
NC_000012.10:g.108518656C>G	NCBI36
NG_007702.1:g.27774C>G , LRG_156:g.27774C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.239C>G	ENSP00000439134.1:p.Thr80Ser
ENST00000546277.6:c.1082C>G	ENSP00000438153.2:p.Thr361Ser
ENST00000636529.2:n.721C>G
ENST00000697195.1:c.*846C>G	ENSP00000513181.1:n.*846C>G
ENST00000697196.1:c.*255C>G	ENSP00000513182.1:n.*255C>G
ENST00000697197.1:n.3111C>G
ENST00000697198.1:n.1466C>G
ENST00000228510.8:c.1082C>G MANE Select	ENSP00000228510.3:p.Thr361Ser
ENST00000636529.1:c.707C>G
ENST00000636996.1:c.930C>G
ENST00000228510.7:c.1082C>G	ENSP00000228510.3:p.Thr361Ser
ENST00000392727.7:c.926C>G	ENSP00000376487.3:p.Thr309Ser
ENST00000447878.6:c.*529C>G	ENSP00000415555.2:n.*529C>G
ENST00000537237.5:c.*755C>G	ENSP00000445382.1:n.*755C>G
ENST00000539575.4:c.1082C>G	ENSP00000443551.2:p.Thr361Ser
ENST00000539696.5:c.239C>G	ENSP00000439134.1:p.Thr80Ser
ENST00000540353.1:n.3315C>G
ENST00000625889.2:c.926C>G	ENSP00000486846.1:p.Thr309Ser
ENST00000629016.2:c.*529C>G	ENSP00000486804.1:n.*529C>G
NM_000431.3:c.1082C>G	NP_000422.1:p.Thr361Ser
NM_001114185.2:c.1082C>G	NP_001107657.1:p.Thr361Ser
NM_001301182.1:c.926C>G	NP_001288111.1:p.Thr309Ser
XM_011538372.1:c.1082C>G	XP_011536674.1:p.Thr361Ser
XM_017019313.2:c.926C>G	XP_016874802.1:p.Thr309Ser
XM_017019314.1:c.1082C>G	XP_016874803.1:p.Thr361Ser
NM_000431.4:c.1082C>G MANE Select	NP_000422.1:p.Thr361Ser
NM_001114185.3:c.1082C>G	NP_001107657.1:p.Thr361Ser
NM_001301182.2:c.926C>G	NP_001288111.1:p.Thr309Ser