Canonical Allele Identifier: CA386649369

Gene: MVK

Linked Data

• MyVariant Identifiers: chr12:g.110029092C>A (hg19) ; chr12:g.109591287C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109591287C>A , CM000674.2:g.109591287C>A	GRCh38
NC_000012.11:g.110029092C>A , CM000674.1:g.110029092C>A	GRCh37
NC_000012.10:g.108513475C>A	NCBI36
NG_007702.1:g.22593C>A , LRG_156:g.22593C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.-29C>A	ENSP00000439134.1:n.-29C>A
ENST00000546277.6:c.815C>A	ENSP00000438153.2:p.Ser272Tyr
ENST00000636529.2:n.454C>A
ENST00000697195.1:c.*579C>A	ENSP00000513181.1:n.*579C>A
ENST00000697196.1:c.903C>A	ENSP00000513182.1:p.Leu301=
ENST00000697197.1:n.2844C>A
ENST00000228510.8:c.815C>A MANE Select	ENSP00000228510.3:p.Ser272Tyr
ENST00000636529.1:c.440C>A
ENST00000636996.1:c.663C>A
ENST00000228510.7:c.815C>A	ENSP00000228510.3:p.Ser272Tyr
ENST00000392727.7:c.659C>A	ENSP00000376487.3:p.Ser220Tyr
ENST00000447878.6:c.*262C>A	ENSP00000415555.2:n.*262C>A
ENST00000537237.5:c.*488C>A	ENSP00000445382.1:n.*488C>A
ENST00000539575.4:c.815C>A	ENSP00000443551.2:p.Ser272Tyr
ENST00000539696.5:c.-29C>A	ENSP00000439134.1:n.-29C>A
ENST00000540353.1:n.3048C>A
ENST00000625889.2:c.659C>A	ENSP00000486846.1:p.Ser220Tyr
ENST00000629016.2:c.*262C>A	ENSP00000486804.1:n.*262C>A
NM_000431.3:c.815C>A	NP_000422.1:p.Ser272Tyr
NM_001114185.2:c.815C>A	NP_001107657.1:p.Ser272Tyr
NM_001301182.1:c.659C>A	NP_001288111.1:p.Ser220Tyr
XM_011538372.1:c.815C>A	XP_011536674.1:p.Ser272Tyr
XM_017019313.2:c.659C>A	XP_016874802.1:p.Ser220Tyr
XM_017019314.1:c.815C>A	XP_016874803.1:p.Ser272Tyr
XM_024448982.1:c.815C>A	XP_024304750.1:p.Ser272Tyr
NM_000431.4:c.815C>A MANE Select	NP_000422.1:p.Ser272Tyr
NM_001114185.3:c.815C>A	NP_001107657.1:p.Ser272Tyr
NM_001301182.2:c.659C>A	NP_001288111.1:p.Ser220Tyr