Canonical Allele Identifier: CA1608636349

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7541631C= , CM000668.2:g.7541631C= GRCh38
NC_000006.11:g.7541864C= , CM000668.1:g.7541864C= GRCh37
NC_000006.10:g.7486863C= NCBI36
NG_008803.1:g.4995C= , LRG_423:g.4995C=

Transcript Alleles

HGVS Amino-acid change
ENST00000710359.1:c.-285C= (DSP) ENSP00000518230.1:n.-285C=
ENST00000379802.7:c.-285C= (DSP) ENSP00000369129.3:n.-285C=
ENST00000418664.2:c.-285C= (DSP) ENSP00000396591.2:n.-285C=
XM_011514323.1:c.-285C= (DSP) XP_011512625.1:n.-285C=
XR_241971.2:n.269-578G= (DSP-AS1)
NM_001008844.2:c.-285C= (DSP) NP_001008844.1:n.-285C=
NM_001319034.1:c.-285C= (DSP) NP_001305963.1:n.-285C=
NM_004415.3:c.-285C= (DSP) NP_004406.2:n.-285C=
XR_241970.4:n.96G= (DSP-AS1)
XR_241971.3:n.270-578G= (DSP-AS1)