Canonical Allele Identifier: CA7345142

Gene: WARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.100342508G>A , CM000676.2:g.100342508G>A	GRCh38
NC_000014.8:g.100808845G>A , CM000676.1:g.100808845G>A	GRCh37
NC_000014.7:g.99878598G>A	NCBI36
NG_029914.1:g.38836C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004184.4:c.1003C>T MANE Select	NP_004175.2:p.Leu335=
ENST00000392882.7:c.1003C>T MANE Select	ENSP00000376620.2:p.Leu335=
NM_004184.3:c.1003C>T	NP_004175.2:p.Leu335=
NM_173701.1:c.1003C>T	NP_776049.1:p.Leu335=
NM_173701.2:c.1003C>T	NP_776049.1:p.Leu335=
NM_213645.1:c.880C>T	NP_998810.1:p.Leu294=
NM_213645.2:c.880C>T	NP_998810.1:p.Leu294=
NM_213646.1:c.880C>T	NP_998811.1:p.Leu294=
NM_213646.2:c.880C>T	NP_998811.1:p.Leu294=
ENST00000344102.9:c.880C>T	ENSP00000339485.5:p.Leu294=
ENST00000355338.6:c.1003C>T	ENSP00000347495.2:p.Leu335=
ENST00000358655.8:c.880C>T	ENSP00000351481.4:p.Leu294=
ENST00000392882.6:c.1003C>T	ENSP00000376620.2:p.Leu335=
ENST00000554601.1:c.261C>T
ENST00000554950.1:n.1015C>T
ENST00000556645.5:c.880C>T	ENSP00000451887.1:p.Leu294=
ENST00000557135.5:c.1003C>T	ENSP00000451460.1:p.Leu335=
ENST00000557614.1:n.27C>T
XM_005268044.2:c.1003C>T	XP_005268101.1:p.Leu335=
XM_005268044.4:c.1003C>T	XP_005268101.1:p.Leu335=
XM_006720249.2:c.1003C>T	XP_006720312.1:p.Leu335=
XM_006720249.3:c.1003C>T	XP_006720312.1:p.Leu335=
XM_011537133.1:c.1003C>T	XP_011535435.1:p.Leu335=
XM_011537133.2:c.1003C>T	XP_011535435.1:p.Leu335=
XM_011537134.1:c.1003C>T	XP_011535436.1:p.Leu335=
XM_011537135.1:c.1003C>T	XP_011535437.1:p.Leu335=
XM_011537136.1:c.880C>T	XP_011535438.1:p.Leu294=
XM_011537136.3:c.880C>T	XP_011535438.1:p.Leu294=
XM_011537137.1:c.880C>T	XP_011535439.1:p.Leu294=
XM_017021627.2:c.1003C>T	XP_016877116.1:p.Leu335=
XM_017021629.1:c.1003C>T	XP_016877118.1:p.Leu335=
XM_024449706.1:c.1003C>T	XP_024305474.1:p.Leu335=
XM_024449707.1:c.1003C>T	XP_024305475.1:p.Leu335=
XM_024449708.1:c.880C>T	XP_024305476.1:p.Leu294=