Canonical Allele Identifier: CA2769903712
Gene: DSP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7553835G>T , CM000668.2:g.7553835G>T GRCh38
NC_000006.11:g.7554068G>T , CM000668.1:g.7554068G>T GRCh37
NC_000006.10:g.7499067G>T NCBI36
NG_008803.1:g.17199G>T , LRG_423:g.17199G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000683682.2:c.171-1883G>T ENSP00000508162.2:n.171-1883G>T
ENST00000710359.1:c.171-1883G>T ENSP00000518230.1:n.171-1883G>T
ENST00000683563.1:n.63-1883G>T
ENST00000683682.1:c.66-1883G>T ENSP00000508162.1:n.66-1883G>T
ENST00000379802.8:c.171-1883G>T MANE Select ENSP00000369129.3:n.171-1883G>T
ENST00000379802.7:c.171-1883G>T ENSP00000369129.3:n.171-1883G>T
ENST00000418664.2:c.171-1883G>T ENSP00000396591.2:n.171-1883G>T
NM_001008844.1:c.171-1883G>T NP_001008844.1:n.171-1883G>T
NM_004415.2:c.171-1883G>T , LRG_423t1:c.171-1883G>T NP_004406.2:n.171-1883G>T
XM_011514323.1:c.171-1883G>T XP_011512625.1:n.171-1883G>T
NM_001008844.2:c.171-1883G>T NP_001008844.1:n.171-1883G>T
NM_001319034.1:c.171-1883G>T NP_001305963.1:n.171-1883G>T
NM_004415.3:c.171-1883G>T NP_004406.2:n.171-1883G>T
NM_004415.4:c.171-1883G>T MANE Select NP_004406.2:n.171-1883G>T
NM_001008844.3:c.171-1883G>T NP_001008844.1:n.171-1883G>T
NM_001319034.2:c.171-1883G>T NP_001305963.1:n.171-1883G>T