Canonical Allele Identifier: CA1956502783

Gene: HTATIP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.20383067T= , CM000673.2:g.20383067T=	GRCh38
NC_000011.9:g.20404613T= , CM000673.1:g.20404613T=	GRCh37
NC_000011.8:g.20361189T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001098522.2:c.591T= MANE Select	NP_001091992.1:p.Ser197=
ENST00000451739.7:c.591T= MANE Select	ENSP00000394259.2:p.Ser197=
NM_001098520.1:c.693T=	NP_001091990.1:p.Ser231=
NM_001098520.2:c.693T=	NP_001091990.1:p.Ser231=
NM_001098521.1:c.591T=	NP_001091991.1:p.Ser197=
NM_001098521.2:c.591T=	NP_001091991.1:p.Ser197=
NM_001098522.1:c.591T=	NP_001091992.1:p.Ser197=
NM_006410.4:c.591T=	NP_006401.3:p.Ser197=
NM_006410.5:c.591T=	NP_006401.3:p.Ser197=
ENST00000419348.6:c.693T=	ENSP00000392985.2:p.Ser231=
ENST00000421577.6:c.591T=	ENSP00000397752.2:p.Ser197=
ENST00000443524.6:c.591T=	ENSP00000387876.2:p.Ser197=
ENST00000451739.6:c.591T=	ENSP00000394259.2:p.Ser197=
ENST00000531058.1:c.453T=	ENSP00000436729.1:p.Ser151=
ENST00000533914.1:n.851T=