Canonical Allele Identifier: CA346211550

Gene: CAD

Linked Data

• MyVariant Identifiers: chr2:g.27454969A>T (hg19) ; chr2:g.27232101A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27232101A>T , CM000664.2:g.27232101A>T	GRCh38
NC_000002.11:g.27454969A>T , CM000664.1:g.27454969A>T	GRCh37
NC_000002.10:g.27308473A>T	NCBI36
NG_046394.1:g.19712A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000264705.9:c.2522A>T MANE Select	ENSP00000264705.3:p.Lys841Met
ENST00000264705.8:c.2522A>T	ENSP00000264705.3:p.Lys841Met
ENST00000403525.5:c.2333A>T	ENSP00000384510.1:p.Lys778Met
ENST00000464159.1:n.270A>T
NM_001306079.1:c.2333A>T	NP_001293008.1:p.Lys778Met
NM_004341.3:c.2522A>T	NP_004332.2:p.Lys841Met
NM_004341.4:c.2522A>T	NP_004332.2:p.Lys841Met
XM_005264555.2:c.2522A>T	XP_005264612.1:p.Lys841Met
XM_005264556.2:c.2522A>T	XP_005264613.1:p.Lys841Met
XM_005264557.2:c.2522A>T	XP_005264614.1:p.Lys841Met
XM_006712101.1:c.2333A>T	XP_006712164.1:p.Lys778Met
XM_006712101.3:c.2333A>T	XP_006712164.1:p.Lys778Met
XM_024453131.1:c.248A>T	XP_024308899.1:p.Lys83Met
NM_004341.5:c.2522A>T MANE Select	NP_004332.2:p.Lys841Met
NM_001306079.2:c.2333A>T	NP_001293008.1:p.Lys778Met