Canonical Allele Identifier: CA7345039

Gene: WARS1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.100337027A>G , CM000676.2:g.100337027A>G	GRCh38
NC_000014.8:g.100803364A>G , CM000676.1:g.100803364A>G	GRCh37
NC_000014.7:g.99873117A>G	NCBI36
NG_029914.1:g.44317T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392882.7:c.1254+35T>C MANE Select	ENSP00000376620.2:n.1254+35T>C
ENST00000344102.9:c.1131+35T>C	ENSP00000339485.5:n.1131+35T>C
ENST00000355338.6:c.1254+35T>C	ENSP00000347495.2:n.1254+35T>C
ENST00000358655.8:c.1131+35T>C	ENSP00000351481.4:n.1131+35T>C
ENST00000392882.6:c.1254+35T>C	ENSP00000376620.2:n.1254+35T>C
ENST00000554950.1:n.1266+35T>C
ENST00000556645.5:c.1131+35T>C	ENSP00000451887.1:n.1131+35T>C
ENST00000557135.5:c.1254+35T>C	ENSP00000451460.1:n.1254+35T>C
ENST00000557614.1:n.313T>C
NM_004184.3:c.1254+35T>C	NP_004175.2:n.1254+35T>C
NM_173701.1:c.1254+35T>C	NP_776049.1:n.1254+35T>C
NM_213645.1:c.1131+35T>C	NP_998810.1:n.1131+35T>C
NM_213646.1:c.1131+35T>C	NP_998811.1:n.1131+35T>C
XM_005268044.2:c.1254+35T>C	XP_005268101.1:n.1254+35T>C
XM_006720249.2:c.1254+35T>C	XP_006720312.1:n.1254+35T>C
XM_011537133.1:c.1254+35T>C	XP_011535435.1:n.1254+35T>C
XM_011537134.1:c.1254+35T>C	XP_011535436.1:n.1254+35T>C
XM_011537135.1:c.1254+35T>C	XP_011535437.1:n.1254+35T>C
XM_011537136.1:c.1131+35T>C	XP_011535438.1:n.1131+35T>C
XM_011537137.1:c.1131+35T>C	XP_011535439.1:n.1131+35T>C
XM_005268044.4:c.1254+35T>C	XP_005268101.1:n.1254+35T>C
XM_006720249.3:c.1254+35T>C	XP_006720312.1:n.1254+35T>C
XM_011537133.2:c.1254+35T>C	XP_011535435.1:n.1254+35T>C
XM_011537136.3:c.1131+35T>C	XP_011535438.1:n.1131+35T>C
XM_017021627.2:c.1254+35T>C	XP_016877116.1:n.1254+35T>C
XM_017021629.1:c.1254+35T>C	XP_016877118.1:n.1254+35T>C
XM_024449706.1:c.1254+35T>C	XP_024305474.1:n.1254+35T>C
XM_024449707.1:c.1254+35T>C	XP_024305475.1:n.1254+35T>C
XM_024449708.1:c.1131+35T>C	XP_024305476.1:n.1131+35T>C
NM_004184.4:c.1254+35T>C MANE Select	NP_004175.2:n.1254+35T>C
NM_173701.2:c.1254+35T>C	NP_776049.1:n.1254+35T>C
NM_213645.2:c.1131+35T>C	NP_998810.1:n.1131+35T>C
NM_213646.2:c.1131+35T>C	NP_998811.1:n.1131+35T>C