Canonical Allele Identifier: CA395729707

Gene: VKORC1

Linked Data

• MyVariant Identifiers: chr16:g.31102576A>G (hg19) ; chr16:g.31091255A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091255A>G , CM000678.2:g.31091255A>G	GRCh38
NC_000016.9:g.31102576A>G , CM000678.1:g.31102576A>G	GRCh37
NC_000016.8:g.31010077A>G	NCBI36
NG_011564.1:g.8701T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000394975.3:c.371T>C MANE Select	ENSP00000378426.2:p.Leu124Pro
ENST00000300851.10:c.432T>C	ENSP00000300851.6:p.Pro144=
ENST00000319788.11:c.453T>C	ENSP00000326135.7:p.Pro151=
ENST00000354895.4:c.261T>C	ENSP00000346969.4:p.Pro87=
ENST00000394971.7:c.465T>C	ENSP00000378422.3:p.Pro155=
ENST00000394975.2:c.371T>C	ENSP00000378426.2:p.Leu124Pro
ENST00000420057.2:c.333T>C
ENST00000472468.1:c.56T>C	ENSP00000458994.1:p.Leu19Pro
ENST00000498155.1:c.468T>C	ENSP00000417662.1:p.Pro156=
ENST00000529564.1:c.283+2057T>C	ENSP00000431371.1:n.283+2057T>C
ENST00000532364.1:c.173+3302T>C	ENSP00000460316.1:n.173+3302T>C
ENST00000533518.5:c.244T>C
NM_001311311.1:c.455T>C	NP_001298240.1:p.Leu152Pro
NM_024006.4:c.371T>C	NP_076869.1:p.Leu124Pro
NM_024006.5:c.371T>C	NP_076869.1:p.Leu124Pro
NM_206824.1:c.261T>C	NP_996560.1:p.Pro87=
NM_206824.2:c.261T>C	NP_996560.1:p.Pro87=
XM_011545944.1:c.371T>C	XP_011544246.1:p.Leu124Pro
XM_011545945.1:c.261T>C	XP_011544247.1:p.Pro87=
XR_950848.1:n.1159T>C
NM_024006.6:c.371T>C MANE Select	NP_076869.1:p.Leu124Pro
NM_001311311.2:c.455T>C	NP_001298240.1:p.Leu152Pro
NM_206824.3:c.261T>C	NP_996560.1:p.Pro87=