Canonical Allele Identifier: CA1608623686

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7568826_7568831delinsACTTTT , CM000668.2:g.7568826_7568831delinsACTTTT	GRCh38
NC_000006.11:g.7569059_7569064delinsACTTTT , CM000668.1:g.7569059_7569064delinsACTTTT	GRCh37
NC_000006.10:g.7514058_7514063delinsACTTTT	NCBI36
NG_008803.1:g.32190_32195delinsACTTTT , LRG_423:g.32190_32195delinsACTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.1419+237_1419+242delinsACTTTT	ENSP00000518230.1:n.1419+237_1419+242delinsACTTTT
ENST00000379802.8:c.1419+237_1419+242delinsACTTTT MANE Select	ENSP00000369129.3:n.1419+237_1419+242delinsACTTTT
ENST00000379802.7:c.1419+237_1419+242delinsACTTTT	ENSP00000369129.3:n.1419+237_1419+242delinsACTTTT
ENST00000418664.2:c.1419+237_1419+242delinsACTTTT	ENSP00000396591.2:n.1419+237_1419+242delinsACTTTT
NM_001008844.1:c.1419+237_1419+242delinsACTTTT	NP_001008844.1:n.1419+237_1419+242delinsACTTTT
NM_004415.2:c.1419+237_1419+242delinsACTTTT , LRG_423t1:c.1419+237_1419+242delinsACTTTT	NP_004406.2:n.1419+237_1419+242delinsACTTTT
XM_011514323.1:c.1419+237_1419+242delinsACTTTT	XP_011512625.1:n.1419+237_1419+242delinsACTTTT
NM_001008844.2:c.1419+237_1419+242delinsACTTTT	NP_001008844.1:n.1419+237_1419+242delinsACTTTT
NM_001319034.1:c.1419+237_1419+242delinsACTTTT	NP_001305963.1:n.1419+237_1419+242delinsACTTTT
NM_004415.3:c.1419+237_1419+242delinsACTTTT	NP_004406.2:n.1419+237_1419+242delinsACTTTT
NM_004415.4:c.1419+237_1419+242delinsACTTTT MANE Select	NP_004406.2:n.1419+237_1419+242delinsACTTTT
NM_001008844.3:c.1419+237_1419+242delinsACTTTT	NP_001008844.1:n.1419+237_1419+242delinsACTTTT
NM_001319034.2:c.1419+237_1419+242delinsACTTTT	NP_001305963.1:n.1419+237_1419+242delinsACTTTT