Canonical Allele Identifier: CA395729653

Gene: VKORC1

Linked Data

• MyVariant Identifiers: chr16:g.31102564A>G (hg19) ; chr16:g.31091243A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091243A>G , CM000678.2:g.31091243A>G	GRCh38
NC_000016.9:g.31102564A>G , CM000678.1:g.31102564A>G	GRCh37
NC_000016.8:g.31010065A>G	NCBI36
NG_011564.1:g.8713T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000394975.3:c.383T>C MANE Select	ENSP00000378426.2:p.Leu128Pro
ENST00000300851.10:c.444T>C	ENSP00000300851.6:p.Ala148=
ENST00000319788.11:c.465T>C	ENSP00000326135.7:p.Ala155=
ENST00000354895.4:c.273T>C	ENSP00000346969.4:p.Ala91=
ENST00000394971.7:c.477T>C	ENSP00000378422.3:p.Ala159=
ENST00000394975.2:c.383T>C	ENSP00000378426.2:p.Leu128Pro
ENST00000420057.2:c.345T>C
ENST00000472468.1:c.68T>C	ENSP00000458994.1:p.Leu23Pro
ENST00000498155.1:c.480T>C	ENSP00000417662.1:p.Ala160=
ENST00000529564.1:c.283+2069T>C	ENSP00000431371.1:n.283+2069T>C
ENST00000532364.1:c.173+3314T>C	ENSP00000460316.1:n.173+3314T>C
ENST00000533518.5:c.256T>C
NM_001311311.1:c.467T>C	NP_001298240.1:p.Leu156Pro
NM_024006.4:c.383T>C	NP_076869.1:p.Leu128Pro
NM_024006.5:c.383T>C	NP_076869.1:p.Leu128Pro
NM_206824.1:c.273T>C	NP_996560.1:p.Ala91=
NM_206824.2:c.273T>C	NP_996560.1:p.Ala91=
XM_011545944.1:c.383T>C	XP_011544246.1:p.Leu128Pro
XM_011545945.1:c.273T>C	XP_011544247.1:p.Ala91=
XR_950848.1:n.1171T>C
NM_024006.6:c.383T>C MANE Select	NP_076869.1:p.Leu128Pro
NM_001311311.2:c.467T>C	NP_001298240.1:p.Leu156Pro
NM_206824.3:c.273T>C	NP_996560.1:p.Ala91=