Canonical Allele Identifier: CA447088644

Gene: DIAPH1

Linked Data

• dbSNP Id: rs71583655
• gnomAD v2: 5-140953581-A-C
• gnomAD v4: 5-141574014-A-C
• MyVariant Identifiers: chr5:g.140953581A>C (hg19) ; chr5:g.141574014A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141574014A>C , CM000667.2:g.141574014A>C	GRCh38
NC_000005.9:g.140953581A>C , CM000667.1:g.140953581A>C	GRCh37
NC_000005.8:g.140933765A>C	NCBI36
NG_011594.1:g.50042T>G
NG_011594.2:g.50042T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389054.8:c.1836T>G MANE Select	ENSP00000373706.4:p.Pro612=
ENST00000647433.1:c.1836T>G	ENSP00000494675.1:p.Pro612=
ENST00000253811.10:c.1704T>G	ENSP00000253811.7:p.Pro568=
ENST00000389054.7:c.1836T>G	ENSP00000373706.4:p.Pro612=
ENST00000389057.9:c.1809T>G	ENSP00000373709.6:p.Pro603=
ENST00000398557.8:c.1836T>G	ENSP00000381565.5:p.Pro612=
ENST00000518047.5:c.1809T>G	ENSP00000428268.2:p.Pro603=
NM_001079812.2:c.1809T>G	NP_001073280.1:p.Pro603=
NM_001314007.1:c.1836T>G	NP_001300936.1:p.Pro612=
NM_005219.4:c.1836T>G	NP_005210.3:p.Pro612=
XM_011537572.1:c.1800T>G	XP_011535874.1:p.Pro600=
XM_011537573.1:c.1770T>G	XP_011535875.1:p.Pro590=
XM_024454384.1:c.1836T>G	XP_024310152.1:p.Pro612=
XM_024454385.1:c.1809T>G	XP_024310153.1:p.Pro603=
XM_024454386.1:c.1800T>G	XP_024310154.1:p.Pro600=
XM_024454387.1:c.1770T>G	XP_024310155.1:p.Pro590=
NM_005219.5:c.1836T>G MANE Select	NP_005210.3:p.Pro612=
NM_001079812.3:c.1809T>G	NP_001073280.1:p.Pro603=
NM_001314007.2:c.1836T>G	NP_001300936.1:p.Pro612=