Canonical Allele Identifier: CA368858347

Gene: DLD

Linked Data

• gnomAD v4: 7-107917374-A-T
• MyVariant Identifiers: chr7:g.107557819A>T (hg19) ; chr7:g.107917374A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107917374A>T , CM000669.2:g.107917374A>T	GRCh38
NC_000007.13:g.107557819A>T , CM000669.1:g.107557819A>T	GRCh37
NC_000007.12:g.107345055A>T	NCBI36
NG_008045.1:g.31234A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.1148A>T MANE Select	ENSP00000205402.3:p.His383Leu
ENST00000205402.9:c.1148A>T	ENSP00000205402.3:p.His383Leu
ENST00000415325.5:c.*822A>T	ENSP00000402593.1:n.*822A>T
ENST00000417551.5:c.1148A>T	ENSP00000390667.1:p.His383Leu
ENST00000437604.6:c.1004A>T	ENSP00000387542.2:p.His335Leu
ENST00000440410.5:c.1079A>T	ENSP00000417016.1:p.His360Leu
NM_000108.4:c.1148A>T	NP_000099.2:p.His383Leu
NM_001289750.1:c.851A>T	NP_001276679.1:p.His284Leu
NM_001289751.1:c.1079A>T	NP_001276680.1:p.His360Leu
NM_001289752.1:c.1004A>T	NP_001276681.1:p.His335Leu
NM_000108.5:c.1148A>T MANE Select	NP_000099.2:p.His383Leu