Canonical Allele Identifier: CA361518632

Gene: DIAPH1

Linked Data

• gnomAD v3: 5-141573792-T-A
• gnomAD v4: 5-141573792-T-A
• MyVariant Identifiers: chr5:g.140953359T>A (hg19) ; chr5:g.141573792T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141573792T>A , CM000667.2:g.141573792T>A	GRCh38
NC_000005.9:g.140953359T>A , CM000667.1:g.140953359T>A	GRCh37
NC_000005.8:g.140933543T>A	NCBI36
NG_011594.1:g.50264A>T
NG_011594.2:g.50264A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389054.8:c.2058A>T MANE Select	ENSP00000373706.4:p.Arg686Ser
ENST00000647433.1:c.2058A>T	ENSP00000494675.1:p.Arg686Ser
ENST00000253811.10:c.1926A>T	ENSP00000253811.7:p.Arg642Ser
ENST00000389054.7:c.2058A>T	ENSP00000373706.4:p.Arg686Ser
ENST00000389057.9:c.2031A>T	ENSP00000373709.6:p.Arg677Ser
ENST00000398557.8:c.2058A>T	ENSP00000381565.5:p.Arg686Ser
ENST00000518047.5:c.2031A>T	ENSP00000428268.2:p.Arg677Ser
NM_001079812.2:c.2031A>T	NP_001073280.1:p.Arg677Ser
NM_001314007.1:c.2058A>T	NP_001300936.1:p.Arg686Ser
NM_005219.4:c.2058A>T	NP_005210.3:p.Arg686Ser
XM_011537572.1:c.2022A>T	XP_011535874.1:p.Arg674Ser
XM_011537573.1:c.1992A>T	XP_011535875.1:p.Arg664Ser
XM_024454384.1:c.2058A>T	XP_024310152.1:p.Arg686Ser
XM_024454385.1:c.2031A>T	XP_024310153.1:p.Arg677Ser
XM_024454386.1:c.2022A>T	XP_024310154.1:p.Arg674Ser
XM_024454387.1:c.1992A>T	XP_024310155.1:p.Arg664Ser
NM_005219.5:c.2058A>T MANE Select	NP_005210.3:p.Arg686Ser
NM_001079812.3:c.2031A>T	NP_001073280.1:p.Arg677Ser
NM_001314007.2:c.2058A>T	NP_001300936.1:p.Arg686Ser