Canonical Allele Identifier: CA1608609972
Gene: DSP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7577058A= , CM000668.2:g.7577058A= GRCh38
NC_000006.11:g.7577291A= , CM000668.1:g.7577291A= GRCh37
NC_000006.10:g.7522290A= NCBI36
NG_008803.1:g.40422A= , LRG_423:g.40422A=

Transcript Alleles

HGVS Amino-acid change
ENST00000710359.1:c.2877+16A= ENSP00000518230.1:n.2877+16A=
ENST00000379802.8:c.2877+16A= MANE Select ENSP00000369129.3:n.2877+16A=
ENST00000379802.7:c.2877+16A= ENSP00000369129.3:n.2877+16A=
ENST00000418664.2:c.2877+16A= ENSP00000396591.2:n.2877+16A=
NM_001008844.1:c.2877+16A= NP_001008844.1:n.2877+16A=
NM_004415.2:c.2877+16A= , LRG_423t1:c.2877+16A= NP_004406.2:n.2877+16A=
XM_011514323.1:c.2877+16A= XP_011512625.1:n.2877+16A=
NM_001008844.2:c.2877+16A= NP_001008844.1:n.2877+16A=
NM_001319034.1:c.2877+16A= NP_001305963.1:n.2877+16A=
NM_004415.3:c.2877+16A= NP_004406.2:n.2877+16A=
NM_004415.4:c.2877+16A= MANE Select NP_004406.2:n.2877+16A=
NM_001008844.3:c.2877+16A= NP_001008844.1:n.2877+16A=
NM_001319034.2:c.2877+16A= NP_001305963.1:n.2877+16A=