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Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.154569608A= , CM000666.2:g.154569608A=
GRCh38
NC_000004.11:g.155490760A= , CM000666.1:g.155490760A=
GRCh37
NC_000004.10:g.155710210A=
NCBI36
NG_008833.1:g.11629A= , LRG_558:g.11629A=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000302068.9:c.1053A=
MANE Select
ENSP00000306099.4:p.Lys351=
ENST00000302068.8:c.1053A=
ENSP00000306099.4:p.Lys351=
ENST00000502545.5:n.939+301A=
ENST00000509493.1:c.396A=
ENSP00000426757.1:p.Lys132=
NM_001184741.1:c.876A=
NP_001171670.1:p.Lys292=
NM_005141.4:c.1053A= , LRG_558t1:c.1053A=
NP_005132.2:p.Lys351=
NM_001382759.1:c.921A=
NP_001369688.1:p.Lys307=
NM_001382760.1:c.1053A=
NP_001369689.1:p.Lys351=
NM_001382761.1:c.1053A=
NP_001369690.1:p.Lys351=
NM_001382762.1:c.753A=
NP_001369691.1:p.Lys251=
NM_001382763.1:c.1044A=
NP_001369692.1:p.Lys348=
NM_001382764.1:c.1053A=
NP_001369693.1:p.Lys351=
NM_001382765.1:c.1053A=
NP_001369694.1:p.Lys351=
NM_005141.5:c.1053A=
MANE Select
NP_005132.2:p.Lys351=