Canonical Allele Identifier: CA447088906

Gene: DIAPH1

Linked Data

• gnomAD v3: 5-141573783-T-A
• gnomAD v4: 5-141573783-T-A
• MyVariant Identifiers: chr5:g.140953350T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141573783T>A , CM000667.2:g.141573783T>A	GRCh38
NC_000005.9:g.140953350T>A , CM000667.1:g.140953350T>A	GRCh37
NC_000005.8:g.140933534T>A	NCBI36
NG_011594.1:g.50273A>T
NG_011594.2:g.50273A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389054.8:c.2067A>T MANE Select	ENSP00000373706.4:p.Pro689=
ENST00000647433.1:c.2067A>T	ENSP00000494675.1:p.Pro689=
ENST00000253811.10:c.1935A>T	ENSP00000253811.7:p.Pro645=
ENST00000389054.7:c.2067A>T	ENSP00000373706.4:p.Pro689=
ENST00000389057.9:c.2040A>T	ENSP00000373709.6:p.Pro680=
ENST00000398557.8:c.2067A>T	ENSP00000381565.5:p.Pro689=
ENST00000518047.5:c.2040A>T	ENSP00000428268.2:p.Pro680=
NM_001079812.2:c.2040A>T	NP_001073280.1:p.Pro680=
NM_001314007.1:c.2067A>T	NP_001300936.1:p.Pro689=
NM_005219.4:c.2067A>T	NP_005210.3:p.Pro689=
XM_011537572.1:c.2031A>T	XP_011535874.1:p.Pro677=
XM_011537573.1:c.2001A>T	XP_011535875.1:p.Pro667=
XM_024454384.1:c.2067A>T	XP_024310152.1:p.Pro689=
XM_024454385.1:c.2040A>T	XP_024310153.1:p.Pro680=
XM_024454386.1:c.2031A>T	XP_024310154.1:p.Pro677=
XM_024454387.1:c.2001A>T	XP_024310155.1:p.Pro667=
NM_005219.5:c.2067A>T MANE Select	NP_005210.3:p.Pro689=
NM_001079812.3:c.2040A>T	NP_001073280.1:p.Pro680=
NM_001314007.2:c.2067A>T	NP_001300936.1:p.Pro689=