Canonical Allele Identifier: CA2576939076
Gene: CAD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27231905_27231909dup , CM000664.2:g.27231905_27231909dup GRCh38
NC_000002.11:g.27454773_27454777dup , CM000664.1:g.27454773_27454777dup GRCh37
NC_000002.10:g.27308277_27308281dup NCBI36
NG_046394.1:g.19516_19520dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000264705.9:c.2401-75_2401-71dup MANE Select ENSP00000264705.3:n.2401-75_2401-71dup
ENST00000264705.8:c.2401-75_2401-71dup ENSP00000264705.3:n.2401-75_2401-71dup
ENST00000403525.5:c.2212-75_2212-71dup ENSP00000384510.1:n.2212-75_2212-71dup
ENST00000464159.1:n.149-75_149-71dup
NM_001306079.1:c.2212-75_2212-71dup NP_001293008.1:n.2212-75_2212-71dup
NM_004341.3:c.2401-75_2401-71dup NP_004332.2:n.2401-75_2401-71dup
NM_004341.4:c.2401-75_2401-71dup NP_004332.2:n.2401-75_2401-71dup
XM_005264555.2:c.2401-75_2401-71dup XP_005264612.1:n.2401-75_2401-71dup
XM_005264556.2:c.2401-75_2401-71dup XP_005264613.1:n.2401-75_2401-71dup
XM_005264557.2:c.2401-75_2401-71dup XP_005264614.1:n.2401-75_2401-71dup
XM_006712101.1:c.2212-75_2212-71dup XP_006712164.1:n.2212-75_2212-71dup
XM_006712101.3:c.2212-75_2212-71dup XP_006712164.1:n.2212-75_2212-71dup
XM_024453131.1:c.127-75_127-71dup XP_024308899.1:n.127-75_127-71dup
NM_004341.5:c.2401-75_2401-71dup MANE Select NP_004332.2:n.2401-75_2401-71dup
NM_001306079.2:c.2212-75_2212-71dup NP_001293008.1:n.2212-75_2212-71dup