Canonical Allele Identifier: CA339687707

Gene: YARS1

Linked Data

• MyVariant Identifiers: chr1:g.33276597C>G (hg19) ; chr1:g.32810996C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.32810996C>G , CM000663.2:g.32810996C>G	GRCh38
NC_000001.10:g.33276597C>G , CM000663.1:g.33276597C>G	GRCh37
NC_000001.9:g.33049184C>G	NCBI36
NG_008408.1:g.12037G>C , LRG_273:g.12037G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000675785.2:c.58-230G>C	ENSP00000502019.1:n.58-230G>C
ENST00000373477.9:c.119G>C MANE Select	ENSP00000362576.4:p.Trp40Ser
ENST00000481895.6:c.119G>C	ENSP00000502016.1:p.Trp40Ser
ENST00000616261.2:c.119G>C	ENSP00000484192.2:p.Trp40Ser
ENST00000674629.1:c.58-4385G>C	ENSP00000502470.1:n.58-4385G>C
ENST00000674654.1:c.119G>C	ENSP00000501729.1:p.Trp40Ser
ENST00000675785.1:c.58-230G>C	ENSP00000502019.1:n.58-230G>C
ENST00000676297.1:c.119G>C	ENSP00000501596.1:p.Trp40Ser
ENST00000373477.8:c.119G>C	ENSP00000362576.4:p.Trp40Ser
ENST00000472692.1:n.652G>C
ENST00000481895.5:n.192G>C
ENST00000616261.1:c.119G>C	ENSP00000484192.1:p.Trp40Ser
NM_003680.3:c.119G>C , LRG_273t1:c.119G>C	NP_003671.1:p.Trp40Ser
XM_011542347.1:c.-250-4385G>C	XP_011540649.1:n.-250-4385G>C
XM_011542348.1:c.-297-4385G>C	XP_011540650.1:n.-297-4385G>C
XM_011542347.2:c.-250-4385G>C	XP_011540649.1:n.-250-4385G>C
XM_017002651.2:c.-559G>C	XP_016858140.1:n.-559G>C
NM_003680.4:c.119G>C MANE Select	NP_003671.1:p.Trp40Ser