Canonical Allele Identifier: CA471092135

Gene: HOGA1

Linked Data

• MyVariant Identifiers: chr10:g.99359878T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.97600121T>C , CM000672.2:g.97600121T>C	GRCh38
NC_000010.10:g.99359878T>C , CM000672.1:g.99359878T>C	GRCh37
NC_000010.9:g.99349868T>C	NCBI36
NG_027922.1:g.20777T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370646.9:c.658T>C MANE Select	ENSP00000359680.4:p.Leu220=
ENST00000370642.4:c.68T>C
ENST00000370646.8:c.658T>C	ENSP00000359680.4:p.Leu220=
ENST00000370647.8:c.212-1736T>C	ENSP00000359681.4:n.212-1736T>C
ENST00000370649.3:c.212-1736T>C	ENSP00000359683.3:n.212-1736T>C
ENST00000465608.1:n.1754T>C
NM_001134670.1:c.212-1736T>C	NP_001128142.1:n.212-1736T>C
NM_138413.3:c.658T>C	NP_612422.2:p.Leu220=
NM_138413.4:c.658T>C MANE Select	NP_612422.2:p.Leu220=
NM_001134670.2:c.212-1736T>C	NP_001128142.1:n.212-1736T>C