Canonical Allele Identifier: CA4025738

Gene: CITED2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139373924G>T , CM000668.2:g.139373924G>T	GRCh38
NC_000006.11:g.139695061G>T , CM000668.1:g.139695061G>T	GRCh37
NC_000006.10:g.139736754G>T	NCBI36
NG_016169.1:g.5725C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.21C>A MANE Select	ENSP00000356623.2:p.Ala7=
ENST00000367651.3:c.21C>A	ENSP00000356623.2:p.Ala7=
ENST00000536159.2:c.21C>A	ENSP00000442831.1:p.Ala7=
ENST00000537332.2:c.36C>A	ENSP00000444198.2:p.Ala12=
ENST00000618718.1:c.21C>A	ENSP00000479918.1:p.Ala7=
NM_001168388.2:c.21C>A	NP_001161860.1:p.Ala7=
NM_001168389.2:c.36C>A	NP_001161861.2:p.Ala12=
NM_006079.4:c.21C>A	NP_006070.2:p.Ala7=
NM_006079.5:c.21C>A MANE Select	NP_006070.2:p.Ala7=
NM_001168388.3:c.21C>A	NP_001161860.1:p.Ala7=
NM_001168389.3:c.36C>A	NP_001161861.2:p.Ala12=