Canonical Allele Identifier: CA1608636347

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7541626T= , CM000668.2:g.7541626T= GRCh38
NC_000006.11:g.7541859T= , CM000668.1:g.7541859T= GRCh37
NC_000006.10:g.7486858T= NCBI36
NG_008803.1:g.4990T= , LRG_423:g.4990T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000710359.1:c.-290T= (DSP) ENSP00000518230.1:n.-290T=
ENST00000379802.7:c.-290T= (DSP) ENSP00000369129.3:n.-290T=
ENST00000418664.2:c.-290T= (DSP) ENSP00000396591.2:n.-290T=
XM_011514323.1:c.-290T= (DSP) XP_011512625.1:n.-290T=
XR_241971.2:n.269-573A= (DSP-AS1)
NM_001008844.2:c.-290T= (DSP) NP_001008844.1:n.-290T=
NM_001319034.1:c.-290T= (DSP) NP_001305963.1:n.-290T=
NM_004415.3:c.-290T= (DSP) NP_004406.2:n.-290T=
XR_241970.4:n.101A= (DSP-AS1)
XR_241971.3:n.270-573A= (DSP-AS1)