Canonical Allele Identifier: CA1779071317
Gene: ANK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.41668500A= , CM000670.2:g.41668500A= GRCh38
NC_000008.10:g.41526018A= , CM000670.1:g.41526018A= GRCh37
NC_000008.9:g.41645175A= NCBI36
NG_012820.1:g.233263T=
NG_012820.2:g.233263T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265709.14:c.5284T= ENSP00000265709.8:p.Trp1762=
ENST00000705521.1:c.5380T= ENSP00000516136.1:p.Trp1794=
ENST00000705522.1:c.5197T= ENSP00000516137.1:p.Trp1733=
ENST00000265709.13:c.5284T= ENSP00000265709.8:p.Trp1762=
ENST00000289734.13:c.5161T= MANE Select ENSP00000289734.8:p.Trp1721=
ENST00000645531.1:c.1175T=
ENST00000265709.12:c.5284T= ENSP00000265709.8:p.Trp1762=
ENST00000289734.11:c.5161T= ENSP00000289734.7:p.Trp1721=
ENST00000347528.8:c.5161T= ENSP00000339620.4:p.Trp1721=
ENST00000518061.1:c.733T=
ENST00000520299.5:c.2639T=
ENST00000524227.5:n.2555T=
NM_000037.3:c.5161T= NP_000028.3:p.Trp1721=
NM_001142446.1:c.5284T= NP_001135918.1:p.Trp1762=
NM_020475.2:c.5161T= NP_065208.2:p.Trp1721=
NM_020476.2:c.5161T= NP_065209.2:p.Trp1721=
NM_020477.2:c.4675T= NP_065210.2:p.Trp1559=
XM_005273476.3:c.5284T= XP_005273533.1:p.Trp1762=
XM_011544490.1:c.5425T= XP_011542792.1:p.Trp1809=
XM_011544491.1:c.5425T= XP_011542793.1:p.Trp1809=
XM_011544492.1:c.5326T= XP_011542794.1:p.Trp1776=
XM_011544493.1:c.5425T= XP_011542795.1:p.Trp1809=
XM_011544494.1:c.5380T= XP_011542796.1:p.Trp1794=
XM_011544495.1:c.5380T= XP_011542797.1:p.Trp1794=
XM_011544496.1:c.5425T= XP_011542798.1:p.Trp1809=
XM_011544497.1:c.5260T= XP_011542799.1:p.Trp1754=
XM_011544498.1:c.5242T= XP_011542800.1:p.Trp1748=
XM_011544499.1:c.5425T= XP_011542801.1:p.Trp1809=
XM_011544500.1:c.5260T= XP_011542802.1:p.Trp1754=
XM_011544501.1:c.5260T= XP_011542803.1:p.Trp1754=
XM_011544502.1:c.5260T= XP_011542804.1:p.Trp1754=
XM_011544503.1:c.4894T= XP_011542805.1:p.Trp1632=
XM_011544504.1:c.4774T= XP_011542806.1:p.Trp1592=
XM_011544505.1:c.4774T= XP_011542807.1:p.Trp1592=
XM_011544506.1:c.4985T= XP_011542808.1:p.Leu1662=
XR_949389.1:n.5016T=
XM_005273476.4:c.5284T= XP_005273533.1:p.Trp1762=
XM_011544490.3:c.5425T= XP_011542792.1:p.Trp1809=
XM_011544491.3:c.5425T= XP_011542793.1:p.Trp1809=
XM_011544494.3:c.5380T= XP_011542796.1:p.Trp1794=
XM_011544495.3:c.5380T= XP_011542797.1:p.Trp1794=
XM_011544496.3:c.5425T= XP_011542798.1:p.Trp1809=
XM_011544500.2:c.5260T= XP_011542802.1:p.Trp1754=
XM_011544501.2:c.5260T= XP_011542803.1:p.Trp1754=
XM_011544502.2:c.5260T= XP_011542804.1:p.Trp1754=
XM_011544503.3:c.4894T= XP_011542805.1:p.Trp1632=
XM_011544504.2:c.4774T= XP_011542806.1:p.Trp1592=
XM_011544505.2:c.4774T= XP_011542807.1:p.Trp1592=
XM_017013319.2:c.5401T= XP_016868808.1:p.Trp1801=
XM_017013320.2:c.5425T= XP_016868809.1:p.Trp1809=
XM_017013321.1:c.5338T= XP_016868810.1:p.Trp1780=
XM_017013322.1:c.5329T= XP_016868811.1:p.Trp1777=
XM_017013323.1:c.5326T= XP_016868812.1:p.Trp1776=
XM_017013324.1:c.5284T= XP_016868813.1:p.Trp1762=
XM_017013325.1:c.5242T= XP_016868814.1:p.Trp1748=
XM_017013326.1:c.5197T= XP_016868815.1:p.Trp1733=
XM_017013327.2:c.4939T= XP_016868816.1:p.Trp1647=
XM_017013328.2:c.4894T= XP_016868817.1:p.Trp1632=
XM_017013329.1:c.4798T= XP_016868818.1:p.Trp1600=
XM_024447128.1:c.5230T= XP_024302896.1:p.Trp1744=
NM_000037.4:c.5161T= MANE Select NP_000028.3:p.Trp1721=
NM_001142446.2:c.5284T= NP_001135918.1:p.Trp1762=
NM_020475.3:c.5161T= NP_065208.2:p.Trp1721=
NM_020476.3:c.5161T= NP_065209.2:p.Trp1721=
NM_020477.3:c.4675T= NP_065210.2:p.Trp1559=