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Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.91234660G= , CM000676.2:g.91234660G=
GRCh38
NC_000014.8:g.91701004G= , CM000676.1:g.91701004G=
GRCh37
NC_000014.7:g.90770757G=
NCBI36
NG_052988.1:g.24221C=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000650645.1:c.391C=
MANE Select
ENSP00000498702.1:p.Gln131=
ENST00000529102.1:c.391C=
ENSP00000432740.1:p.Gln131=
ENST00000531499.2:c.391C=
ENSP00000434045.2:p.Gln131=
ENST00000535815.5:c.391C=
ENSP00000440797.1:p.Gln131=
NM_001177676.1:c.391C=
NP_001171147.1:p.Gln131=
NM_003485.3:c.391C=
NP_003476.3:p.Gln131=
XM_005268110.3:c.421C=
XP_005268167.1:p.Gln141=
XM_005268111.2:c.421C=
XP_005268168.1:p.Gln141=
XM_005268112.2:c.421C=
XP_005268169.1:p.Gln141=
XM_006720262.2:c.421C=
XP_006720325.1:p.Gln141=
XM_011537196.1:c.421C=
XP_011535498.1:p.Gln141=
XM_011537197.1:c.421C=
XP_011535499.1:p.Gln141=
XM_011537198.1:c.421C=
XP_011535500.1:p.Gln141=
XM_011537199.1:c.421C=
XP_011535501.1:p.Gln141=
XM_011537200.1:c.421C=
XP_011535502.1:p.Gln141=
NM_001348437.1:c.391C=
NP_001335366.1:p.Gln131=
XM_005268110.4:c.421C=
XP_005268167.1:p.Gln141=
XM_005268111.3:c.421C=
XP_005268168.1:p.Gln141=
XM_005268112.3:c.421C=
XP_005268169.1:p.Gln141=
XM_006720262.3:c.421C=
XP_006720325.1:p.Gln141=
XM_011537196.2:c.421C=
XP_011535498.1:p.Gln141=
XM_011537197.3:c.421C=
XP_011535499.1:p.Gln141=
XM_011537198.2:c.421C=
XP_011535500.1:p.Gln141=
XM_011537199.2:c.421C=
XP_011535501.1:p.Gln141=
NM_001177676.2:c.391C=
MANE Select
NP_001171147.1:p.Gln131=