Canonical Allele Identifier: CA425379612

Gene: CAD

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27217866_27217868del , CM000664.2:g.27217866_27217868del	GRCh38
NC_000002.11:g.27440734_27440736del , CM000664.1:g.27440734_27440736del	GRCh37
NC_000002.10:g.27294238_27294240del	NCBI36
NG_046394.1:g.5477_5479del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264705.9:c.83-11_83-9del MANE Select	ENSP00000264705.3:n.83-11_83-9del
ENST00000264705.8:c.83-11_83-9del	ENSP00000264705.3:n.83-11_83-9del
ENST00000403525.5:c.83-11_83-9del	ENSP00000384510.1:n.83-11_83-9del
NM_001306079.1:c.83-11_83-9del	NP_001293008.1:n.83-11_83-9del
NM_004341.3:c.83-11_83-9del	NP_004332.2:n.83-11_83-9del
NM_004341.4:c.83-11_83-9del	NP_004332.2:n.83-11_83-9del
XM_005264555.2:c.83-11_83-9del	XP_005264612.1:n.83-11_83-9del
XM_005264556.2:c.83-11_83-9del	XP_005264613.1:n.83-11_83-9del
XM_005264557.2:c.83-11_83-9del	XP_005264614.1:n.83-11_83-9del
XM_006712101.1:c.83-11_83-9del	XP_006712164.1:n.83-11_83-9del
XM_006712101.3:c.83-11_83-9del	XP_006712164.1:n.83-11_83-9del
NM_004341.5:c.83-11_83-9del MANE Select	NP_004332.2:n.83-11_83-9del
NM_001306079.2:c.83-11_83-9del	NP_001293008.1:n.83-11_83-9del