Canonical Allele Identifier: CA1608636633

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7541907C= , CM000668.2:g.7541907C= GRCh38
NC_000006.11:g.7542140C= , CM000668.1:g.7542140C= GRCh37
NC_000006.10:g.7487139C= NCBI36
NG_008803.1:g.5271C= , LRG_423:g.5271C=

Transcript Alleles

HGVS Amino-acid change
ENST00000683682.2:c.-9C= (DSP) ENSP00000508162.2:n.-9C=
ENST00000710359.1:c.-9C= (DSP) ENSP00000518230.1:n.-9C=
ENST00000379802.8:c.-9C= (DSP) MANE Select ENSP00000369129.3:n.-9C=
ENST00000379802.7:c.-9C= (DSP) ENSP00000369129.3:n.-9C=
ENST00000418664.2:c.-9C= (DSP) ENSP00000396591.2:n.-9C=
NM_001008844.1:c.-9C= (DSP) NP_001008844.1:n.-9C=
NM_004415.2:c.-9C= , LRG_423t1:c.-9C= (DSP) NP_004406.2:n.-9C=
XM_011514323.1:c.-9C= (DSP) XP_011512625.1:n.-9C=
XR_241971.2:n.269-854G= (DSP-AS1)
NM_001008844.2:c.-9C= (DSP) NP_001008844.1:n.-9C=
NM_001319034.1:c.-9C= (DSP) NP_001305963.1:n.-9C=
NM_004415.3:c.-9C= (DSP) NP_004406.2:n.-9C=
XR_241971.3:n.270-854G= (DSP-AS1)
NM_004415.4:c.-9C= (DSP) MANE Select NP_004406.2:n.-9C=
NM_001008844.3:c.-9C= (DSP) NP_001008844.1:n.-9C=
NM_001319034.2:c.-9C= (DSP) NP_001305963.1:n.-9C=