Canonical Allele Identifier: CA386650809

Gene: MVK

Linked Data

• MyVariant Identifiers: chr12:g.110032932A>T (hg19) ; chr12:g.109595127A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109595127A>T , CM000674.2:g.109595127A>T	GRCh38
NC_000012.11:g.110032932A>T , CM000674.1:g.110032932A>T	GRCh37
NC_000012.10:g.108517315A>T	NCBI36
NG_007702.1:g.26433A>T , LRG_156:g.26433A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.142A>T	ENSP00000439134.1:p.Ser48Cys
ENST00000546277.6:c.985A>T	ENSP00000438153.2:p.Ser329Cys
ENST00000636529.2:n.624A>T
ENST00000697195.1:c.*749A>T	ENSP00000513181.1:n.*749A>T
ENST00000697196.1:c.*158A>T	ENSP00000513182.1:n.*158A>T
ENST00000697197.1:n.3014A>T
ENST00000697198.1:n.1369A>T
ENST00000228510.8:c.985A>T MANE Select	ENSP00000228510.3:p.Ser329Cys
ENST00000636529.1:c.610A>T
ENST00000636996.1:c.833A>T
ENST00000228510.7:c.985A>T	ENSP00000228510.3:p.Ser329Cys
ENST00000392727.7:c.829A>T	ENSP00000376487.3:p.Ser277Cys
ENST00000447878.6:c.*432A>T	ENSP00000415555.2:n.*432A>T
ENST00000537237.5:c.*658A>T	ENSP00000445382.1:n.*658A>T
ENST00000539575.4:c.985A>T	ENSP00000443551.2:p.Ser329Cys
ENST00000539696.5:c.142A>T	ENSP00000439134.1:p.Ser48Cys
ENST00000540353.1:n.3218A>T
ENST00000625889.2:c.829A>T	ENSP00000486846.1:p.Ser277Cys
ENST00000629016.2:c.*432A>T	ENSP00000486804.1:n.*432A>T
NM_000431.3:c.985A>T	NP_000422.1:p.Ser329Cys
NM_001114185.2:c.985A>T	NP_001107657.1:p.Ser329Cys
NM_001301182.1:c.829A>T	NP_001288111.1:p.Ser277Cys
XM_011538372.1:c.985A>T	XP_011536674.1:p.Ser329Cys
XM_017019313.2:c.829A>T	XP_016874802.1:p.Ser277Cys
XM_017019314.1:c.985A>T	XP_016874803.1:p.Ser329Cys
NM_000431.4:c.985A>T MANE Select	NP_000422.1:p.Ser329Cys
NM_001114185.3:c.985A>T	NP_001107657.1:p.Ser329Cys
NM_001301182.2:c.829A>T	NP_001288111.1:p.Ser277Cys