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Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.23814189A= , CM000666.2:g.23814189A=
GRCh38
NC_000004.11:g.23815812A= , CM000666.1:g.23815812A=
GRCh37
NC_000004.10:g.23424910A=
NCBI36
NG_028250.1:g.80889T=
NG_028250.2:g.663787T=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000264867.7:c.1294T=
MANE Select
ENSP00000264867.2:p.Cys432=
ENST00000264867.6:c.1294T=
ENSP00000264867.2:p.Cys432=
ENST00000506055.5:c.*509T=
ENSP00000423075.1:n.*509T=
ENST00000509702.5:n.1334T=
ENST00000613098.4:c.913T=
ENSP00000481498.1:p.Cys305=
NM_013261.3:c.1294T=
NP_037393.1:p.Cys432=
XM_005248130.2:c.1309T=
XP_005248187.1:p.Cys437=
XM_005248131.3:c.1306T=
XP_005248188.1:p.Cys436=
XM_005248132.1:c.1285T=
XP_005248189.1:p.Cys429=
XM_005248134.3:c.1309T=
XP_005248191.1:p.Cys437=
XM_011513764.1:c.1294T=
XP_011512066.1:p.Cys432=
XM_011513765.1:c.1258T=
XP_011512067.1:p.Cys420=
XM_011513766.1:c.1189T=
XP_011512068.1:p.Cys397=
XM_011513767.1:c.1189T=
XP_011512069.1:p.Cys397=
XM_011513768.1:c.1189T=
XP_011512070.1:p.Cys397=
XM_011513769.1:c.1309T=
XP_011512071.1:p.Cys437=
XM_011513770.1:c.913T=
XP_011512072.1:p.Cys305=
XM_011513771.1:c.913T=
XP_011512073.1:p.Cys305=
NM_001330751.1:c.1309T=
NP_001317680.1:p.Cys437=
NM_001330752.1:c.1258T=
NP_001317681.1:p.Cys420=
NM_001330753.1:c.913T=
NP_001317682.1:p.Cys305=
NM_001354825.1:c.1309T=
NP_001341754.1:p.Cys437=
NM_001354826.1:c.913T=
NP_001341755.1:p.Cys305=
NM_001354827.1:c.1309T=
NP_001341756.1:p.Cys437=
NM_013261.4:c.1294T=
NP_037393.1:p.Cys432=
NR_148981.1:n.1821T=
NR_148982.1:n.1894T=
NR_148983.1:n.2047T=
NR_148984.1:n.1445T=
NR_148985.1:n.1959T=
NR_148986.1:n.1964T=
NR_148987.1:n.2046T=
XM_005248131.5:c.1306T=
XP_005248188.1:p.Cys436=
XM_005248134.4:c.1309T=
XP_005248191.1:p.Cys437=
XM_011513769.2:c.1309T=
XP_011512071.1:p.Cys437=
XM_024453878.1:c.1309T=
XP_024309646.1:p.Cys437=
NM_013261.5:c.1294T=
MANE Select
NP_037393.1:p.Cys432=
NM_001330751.2:c.1309T=
NP_001317680.1:p.Cys437=
NM_001330752.2:c.1258T=
NP_001317681.1:p.Cys420=
NM_001354825.2:c.1309T=
NP_001341754.1:p.Cys437=
NM_001354826.2:c.913T=
NP_001341755.1:p.Cys305=
NM_001354827.2:c.1309T=
NP_001341756.1:p.Cys437=
NR_148981.2:n.1897T=
NR_148982.2:n.1970T=
NR_148983.2:n.2123T=
NR_148984.2:n.1415T=
NR_148985.2:n.2035T=
NR_148986.2:n.2040T=
NR_148987.2:n.2122T=
NM_001330753.2:c.913T=
NP_001317682.1:p.Cys305=