Canonical Allele Identifier: CA744903

Gene: YARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.32779484C>T , CM000663.2:g.32779484C>T	GRCh38
NC_000001.10:g.33245085C>T , CM000663.1:g.33245085C>T	GRCh37
NC_000001.9:g.33017672C>T	NCBI36
NG_008408.1:g.43549G>A , LRG_273:g.43549G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675785.2:c.1227G>A	ENSP00000502019.1:p.Pro409=
ENST00000373477.9:c.1374G>A MANE Select	ENSP00000362576.4:p.Pro458=
ENST00000674629.1:c.*922G>A	ENSP00000502470.1:n.*922G>A
ENST00000674654.1:c.*1334G>A	ENSP00000501729.1:n.*1334G>A
ENST00000675785.1:c.1227G>A	ENSP00000502019.1:p.Pro409=
ENST00000676297.1:c.*1548G>A	ENSP00000501596.1:n.*1548G>A
ENST00000373477.8:c.1374G>A	ENSP00000362576.4:p.Pro458=
ENST00000469100.5:n.1290G>A
ENST00000478828.1:n.841G>A
ENST00000487404.5:n.1684G>A
ENST00000490826.1:n.1228G>A
NM_003680.3:c.1374G>A , LRG_273t1:c.1374G>A	NP_003671.1:p.Pro458=
XM_011542347.1:c.744G>A	XP_011540649.1:p.Pro248=
XM_011542348.1:c.744G>A	XP_011540650.1:p.Pro248=
XM_011542347.2:c.744G>A	XP_011540649.1:p.Pro248=
XM_017002651.2:c.744G>A	XP_016858140.1:p.Pro248=
NM_003680.4:c.1374G>A MANE Select	NP_003671.1:p.Pro458=