Canonical Allele Identifier: CA446854590

Gene: DIAPH1

Linked Data

• MyVariant Identifiers: chr5:g.140903753C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141524186C>T , CM000667.2:g.141524186C>T	GRCh38
NC_000005.9:g.140903753C>T , CM000667.1:g.140903753C>T	GRCh37
NC_000005.8:g.140883937C>T	NCBI36
NG_011594.1:g.99870G>A
NG_011594.2:g.99870G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389054.8:c.3618G>A MANE Select	ENSP00000373706.4:p.Leu1206=
ENST00000448451.6:c.24G>A	ENSP00000408159.2:p.Leu8=
ENST00000643312.1:c.24G>A	ENSP00000495191.1:p.Leu8=
ENST00000643718.1:n.98G>A
ENST00000647433.1:c.3618G>A	ENSP00000494675.1:p.Leu1206=
ENST00000253811.10:c.3486G>A	ENSP00000253811.7:p.Leu1162=
ENST00000389054.7:c.3618G>A	ENSP00000373706.4:p.Leu1206=
ENST00000389057.9:c.3591G>A	ENSP00000373709.6:p.Leu1197=
ENST00000398557.8:c.3618G>A	ENSP00000381565.5:p.Leu1206=
ENST00000448451.5:c.154G>A
ENST00000468119.3:n.139G>A
ENST00000476339.1:n.570G>A
ENST00000518047.5:c.3591G>A	ENSP00000428268.2:p.Leu1197=
NM_001079812.2:c.3591G>A	NP_001073280.1:p.Leu1197=
NM_001314007.1:c.3618G>A	NP_001300936.1:p.Leu1206=
NM_005219.4:c.3618G>A	NP_005210.3:p.Leu1206=
XM_011537572.1:c.3582G>A	XP_011535874.1:p.Leu1194=
XM_011537573.1:c.3552G>A	XP_011535875.1:p.Leu1184=
XM_024454384.1:c.3741G>A	XP_024310152.1:p.Leu1247=
XM_024454385.1:c.3714G>A	XP_024310153.1:p.Leu1238=
XM_024454386.1:c.3705G>A	XP_024310154.1:p.Leu1235=
XM_024454387.1:c.3675G>A	XP_024310155.1:p.Leu1225=
NM_005219.5:c.3618G>A MANE Select	NP_005210.3:p.Leu1206=
NM_001079812.3:c.3591G>A	NP_001073280.1:p.Leu1197=
NM_001314007.2:c.3618G>A	NP_001300936.1:p.Leu1206=