Canonical Allele Identifier: CA1608620321
Gene: DSP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7567252A= , CM000668.2:g.7567252A= GRCh38
NC_000006.11:g.7567485A= , CM000668.1:g.7567485A= GRCh37
NC_000006.10:g.7512484A= NCBI36
NG_008803.1:g.30616A= , LRG_423:g.30616A=

Transcript Alleles

HGVS Amino-acid change
ENST00000710359.1:c.1045-102A= ENSP00000518230.1:n.1045-102A=
ENST00000682228.1:n.369-102A=
ENST00000379802.8:c.1045-102A= MANE Select ENSP00000369129.3:n.1045-102A=
ENST00000379802.7:c.1045-102A= ENSP00000369129.3:n.1045-102A=
ENST00000418664.2:c.1045-102A= ENSP00000396591.2:n.1045-102A=
NM_001008844.1:c.1045-102A= NP_001008844.1:n.1045-102A=
NM_004415.2:c.1045-102A= , LRG_423t1:c.1045-102A= NP_004406.2:n.1045-102A=
XM_011514323.1:c.1045-102A= XP_011512625.1:n.1045-102A=
NM_001008844.2:c.1045-102A= NP_001008844.1:n.1045-102A=
NM_001319034.1:c.1045-102A= NP_001305963.1:n.1045-102A=
NM_004415.3:c.1045-102A= NP_004406.2:n.1045-102A=
NM_004415.4:c.1045-102A= MANE Select NP_004406.2:n.1045-102A=
NM_001008844.3:c.1045-102A= NP_001008844.1:n.1045-102A=
NM_001319034.2:c.1045-102A= NP_001305963.1:n.1045-102A=