Canonical Allele Identifier: CA1608636431

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7541726G= , CM000668.2:g.7541726G= GRCh38
NC_000006.11:g.7541959G= , CM000668.1:g.7541959G= GRCh37
NC_000006.10:g.7486958G= NCBI36
NG_008803.1:g.5090G= , LRG_423:g.5090G=

Transcript Alleles

HGVS Amino-acid change
ENST00000683682.2:c.-190G= (DSP) ENSP00000508162.2:n.-190G=
ENST00000710359.1:c.-190G= (DSP) ENSP00000518230.1:n.-190G=
ENST00000379802.8:c.-190G= (DSP) MANE Select ENSP00000369129.3:n.-190G=
ENST00000379802.7:c.-190G= (DSP) ENSP00000369129.3:n.-190G=
ENST00000418664.2:c.-190G= (DSP) ENSP00000396591.2:n.-190G=
NM_001008844.1:c.-190G= (DSP) NP_001008844.1:n.-190G=
NM_004415.2:c.-190G= , LRG_423t1:c.-190G= (DSP) NP_004406.2:n.-190G=
XM_011514323.1:c.-190G= (DSP) XP_011512625.1:n.-190G=
XR_241971.2:n.269-673C= (DSP-AS1)
NM_001008844.2:c.-190G= (DSP) NP_001008844.1:n.-190G=
NM_001319034.1:c.-190G= (DSP) NP_001305963.1:n.-190G=
NM_004415.3:c.-190G= (DSP) NP_004406.2:n.-190G=
XR_241970.4:n.1C= (DSP-AS1)
XR_241971.3:n.270-673C= (DSP-AS1)
NM_004415.4:c.-190G= (DSP) MANE Select NP_004406.2:n.-190G=
NM_001008844.3:c.-190G= (DSP) NP_001008844.1:n.-190G=
NM_001319034.2:c.-190G= (DSP) NP_001305963.1:n.-190G=