Canonical Allele Identifier: CA2553443057

Gene: DLD

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107917323_107917324insCAAT , CM000669.2:g.107917323_107917324insCAAT	GRCh38
NC_000007.13:g.107557768_107557769insCAAT , CM000669.1:g.107557768_107557769insCAAT	GRCh37
NC_000007.12:g.107345004_107345005insCAAT	NCBI36
NG_008045.1:g.31183_31184insCAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.1097_1098insCAAT MANE Select	ENSP00000205402.3:p.Glu367AsnfsTer4
ENST00000205402.9:c.1097_1098insCAAT	ENSP00000205402.3:p.Glu367AsnfsTer4
ENST00000415325.5:c.*771_*772insCAAT	ENSP00000402593.1:n.*771_*772insCAAT
ENST00000417551.5:c.1097_1098insCAAT	ENSP00000390667.1:p.Glu367AsnfsTer4
ENST00000437604.6:c.953_954insCAAT	ENSP00000387542.2:p.Glu319AsnfsTer4
ENST00000440410.5:c.1028_1029insCAAT	ENSP00000417016.1:p.Glu344AsnfsTer4
NM_000108.4:c.1097_1098insCAAT	NP_000099.2:p.Glu367AsnfsTer4
NM_001289750.1:c.800_801insCAAT	NP_001276679.1:p.Glu268AsnfsTer4
NM_001289751.1:c.1028_1029insCAAT	NP_001276680.1:p.Glu344AsnfsTer4
NM_001289752.1:c.953_954insCAAT	NP_001276681.1:p.Glu319AsnfsTer4
NM_000108.5:c.1097_1098insCAAT MANE Select	NP_000099.2:p.Glu367AsnfsTer4