Canonical Allele Identifier: CA395729985

Gene: VKORC1

Linked Data

• dbSNP Id: rs1163093744
• gnomAD v2: 16-31102634-G-A
• gnomAD v3: 16-31091313-G-A
• gnomAD v4: 16-31091313-G-A
• MyVariant Identifiers: chr16:g.31102634G>A (hg19) ; chr16:g.31091313G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091313G>A , CM000678.2:g.31091313G>A	GRCh38
NC_000016.9:g.31102634G>A , CM000678.1:g.31102634G>A	GRCh37
NC_000016.8:g.31010135G>A	NCBI36
NG_011564.1:g.8643C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.313C>T MANE Select	ENSP00000378426.2:p.Leu105=
ENST00000300851.10:c.374C>T	ENSP00000300851.6:p.Pro125Leu
ENST00000319788.11:c.395C>T	ENSP00000326135.7:p.Pro132Leu
ENST00000354895.4:c.203C>T	ENSP00000346969.4:p.Pro68Leu
ENST00000394971.7:c.407C>T	ENSP00000378422.3:p.Pro136Leu
ENST00000394975.2:c.313C>T	ENSP00000378426.2:p.Leu105=
ENST00000420057.2:c.275C>T
ENST00000472468.1:c.-3C>T	ENSP00000458994.1:n.-3C>T
ENST00000498155.1:c.410C>T	ENSP00000417662.1:p.Pro137Leu
ENST00000529564.1:c.283+1999C>T	ENSP00000431371.1:n.283+1999C>T
ENST00000532364.1:c.173+3244C>T	ENSP00000460316.1:n.173+3244C>T
ENST00000533518.5:c.186C>T
NM_001311311.1:c.397C>T	NP_001298240.1:p.Leu133=
NM_024006.4:c.313C>T	NP_076869.1:p.Leu105=
NM_024006.5:c.313C>T	NP_076869.1:p.Leu105=
NM_206824.1:c.203C>T	NP_996560.1:p.Pro68Leu
NM_206824.2:c.203C>T	NP_996560.1:p.Pro68Leu
XM_011545944.1:c.313C>T	XP_011544246.1:p.Leu105=
XM_011545945.1:c.203C>T	XP_011544247.1:p.Pro68Leu
XR_950848.1:n.1101C>T
NM_024006.6:c.313C>T MANE Select	NP_076869.1:p.Leu105=
NM_001311311.2:c.397C>T	NP_001298240.1:p.Leu133=
NM_206824.3:c.203C>T	NP_996560.1:p.Pro68Leu