Canonical Allele Identifier: CA6564574
Community Standard Title: NM_173602.3(DIP2B):c.1632G>A (p.Ser544=)
Gene: DIP2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.50691129G>A , CM000674.2:g.50691129G>A GRCh38
NC_000012.11:g.51084912G>A , CM000674.1:g.51084912G>A GRCh37
NC_000012.10:g.49371179G>A NCBI36
NG_021196.1:g.191145G>A

Transcript Alleles

HGVS Amino-acid Change
NM_173602.3:c.1632G>A MANE Select NP_775873.2:p.Ser544=
ENST00000301180.10:c.1632G>A MANE Select ENSP00000301180.5:p.Ser544=
NM_173602.2:c.1632G>A NP_775873.2:p.Ser544=
ENST00000301180.9:c.1632G>A ENSP00000301180.5:p.Ser544=
ENST00000546732.1:c.182-1820G>A
XM_005269044.1:c.1635G>A XP_005269101.1:p.Ser545=
XM_006719520.2:c.1662G>A XP_006719583.1:p.Ser554=
XM_006719521.2:c.1449G>A XP_006719584.1:p.Ser483=
XM_006719522.2:c.1281G>A XP_006719585.1:p.Ser427=
XM_011538594.1:c.1665G>A XP_011536896.1:p.Ser555=
XM_011538595.1:c.1585-4138G>A XP_011536897.1:n.1585-4138G>A
XM_011538596.1:c.1452G>A XP_011536898.1:p.Ser484=