Canonical Allele Identifier: CA2644703901

Gene: YARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.32782558C>T , CM000663.2:g.32782558C>T	GRCh38
NC_000001.10:g.33248159C>T , CM000663.1:g.33248159C>T	GRCh37
NC_000001.9:g.33020746C>T	NCBI36
NG_008408.1:g.40475G>A , LRG_273:g.40475G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003680.4:c.907-19G>A MANE Select	NP_003671.1:n.907-19G>A
ENST00000373477.9:c.907-19G>A MANE Select	ENSP00000362576.4:n.907-19G>A
NM_003680.3:c.907-19G>A , LRG_273t1:c.907-19G>A	NP_003671.1:n.907-19G>A
ENST00000373477.8:c.907-19G>A	ENSP00000362576.4:n.907-19G>A
ENST00000478828.1:n.374-19G>A
ENST00000487404.5:n.1198G>A
ENST00000616261.1:c.907-19G>A	ENSP00000484192.1:n.907-19G>A
ENST00000674629.1:c.*455-19G>A	ENSP00000502470.1:n.*455-19G>A
ENST00000674654.1:c.*867-19G>A	ENSP00000501729.1:n.*867-19G>A
ENST00000675785.1:c.760-19G>A	ENSP00000502019.1:n.760-19G>A
ENST00000675785.2:c.760-19G>A	ENSP00000502019.1:n.760-19G>A
ENST00000676297.1:c.*1081-19G>A	ENSP00000501596.1:n.*1081-19G>A
XM_011542347.1:c.277-19G>A	XP_011540649.1:n.277-19G>A
XM_011542347.2:c.277-19G>A	XP_011540649.1:n.277-19G>A
XM_011542348.1:c.277-19G>A	XP_011540650.1:n.277-19G>A
XM_017002651.2:c.277-19G>A	XP_016858140.1:n.277-19G>A