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Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.43192400C= , CM000670.2:g.43192400C=
GRCh38
NC_000008.10:g.43047543C= , CM000670.1:g.43047543C=
GRCh37
NC_000008.9:g.43166700C=
NCBI36
NG_009552.1:g.56952C=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000379644.9:c.1347C=
MANE Select
ENSP00000368965.4:p.Asp449=
ENST00000379644.8:c.1347C=
ENSP00000368965.4:p.Asp449=
ENST00000520678.1:n.280C=
ENST00000521576.1:c.498C=
ENSP00000429029.1:p.Asp166=
ENST00000524016.5:c.451C=
NM_152419.2:c.1347C=
NP_689632.2:p.Asp449=
XM_005273409.1:c.1347C=
XP_005273466.1:p.Asp449=
XM_005273410.1:c.1347C=
XP_005273467.1:p.Asp449=
XM_005273411.1:c.1155C=
XP_005273468.1:p.Asp385=
XM_005273412.2:c.1347C=
XP_005273469.1:p.Asp449=
NM_001363227.1:c.1347C=
NP_001350156.1:p.Asp449=
NM_001363228.1:c.1155C=
NP_001350157.1:p.Asp385=
NM_001363229.1:c.483C=
NP_001350158.1:p.Asp161=
XM_005273412.4:c.1347C=
XP_005273469.1:p.Asp449=
NM_152419.3:c.1347C=
MANE Select
NP_689632.2:p.Asp449=
NM_001363227.2:c.1347C=
NP_001350156.1:p.Asp449=
NM_001363228.2:c.1155C=
NP_001350157.1:p.Asp385=
NM_001363229.2:c.483C=
NP_001350158.1:p.Asp161=