Canonical Allele Identifier: CA352197

Gene: LYRM7 HINT1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.131187114dup , CM000667.2:g.131187114dup	GRCh38
NC_000005.9:g.130522807dup , CM000667.1:g.130522807dup	GRCh37
NC_000005.8:g.130550706dup	NCBI36
NG_034163.1:g.21201dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379380.9:c.244+5dup (LYRM7) MANE Select	ENSP00000368688.4:n.244+5dup
ENST00000506207.2:n.109-15381dup (HINT1)
ENST00000379380.8:c.244+5dup (LYRM7)	ENSP00000368688.4:n.244+5dup
ENST00000507584.1:c.162+4815dup (LYRM7)	ENSP00000423991.1:n.162+4815dup
ENST00000510516.5:c.91+6947dup (LYRM7)	ENSP00000423283.1:n.91+6947dup
NM_001293735.1:c.162+4815dup (LYRM7)	NP_001280664.1:n.162+4815dup
NM_181705.3:c.244+5dup (LYRM7)	NP_859056.2:n.244+5dup
NR_121658.1:n.198+6947dup (LYRM7)
NM_181705.4:c.244+5dup (LYRM7) MANE Select	NP_859056.2:n.244+5dup
NM_001293735.2:c.162+4815dup (LYRM7)	NP_001280664.1:n.162+4815dup
NR_121658.2:n.168+6947dup (LYRM7)