Canonical Allele Identifier: CA1608620443

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7567324_7567327delinsGCTA , CM000668.2:g.7567324_7567327delinsGCTA	GRCh38
NC_000006.11:g.7567557_7567560delinsGCTA , CM000668.1:g.7567557_7567560delinsGCTA	GRCh37
NC_000006.10:g.7512556_7512559delinsGCTA	NCBI36
NG_008803.1:g.30688_30691delinsGCTA , LRG_423:g.30688_30691delinsGCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.1045-30_1045-27delinsGCTA	ENSP00000518230.1:n.1045-30_1045-27delinsGCTA
ENST00000682228.1:n.369-30_369-27delinsGCTA
ENST00000379802.8:c.1045-30_1045-27delinsGCTA MANE Select	ENSP00000369129.3:n.1045-30_1045-27delinsGCTA
ENST00000379802.7:c.1045-30_1045-27delinsGCTA	ENSP00000369129.3:n.1045-30_1045-27delinsGCTA
ENST00000418664.2:c.1045-30_1045-27delinsGCTA	ENSP00000396591.2:n.1045-30_1045-27delinsGCTA
NM_001008844.1:c.1045-30_1045-27delinsGCTA	NP_001008844.1:n.1045-30_1045-27delinsGCTA
NM_004415.2:c.1045-30_1045-27delinsGCTA , LRG_423t1:c.1045-30_1045-27delinsGCTA	NP_004406.2:n.1045-30_1045-27delinsGCTA
XM_011514323.1:c.1045-30_1045-27delinsGCTA	XP_011512625.1:n.1045-30_1045-27delinsGCTA
NM_001008844.2:c.1045-30_1045-27delinsGCTA	NP_001008844.1:n.1045-30_1045-27delinsGCTA
NM_001319034.1:c.1045-30_1045-27delinsGCTA	NP_001305963.1:n.1045-30_1045-27delinsGCTA
NM_004415.3:c.1045-30_1045-27delinsGCTA	NP_004406.2:n.1045-30_1045-27delinsGCTA
NM_004415.4:c.1045-30_1045-27delinsGCTA MANE Select	NP_004406.2:n.1045-30_1045-27delinsGCTA
NM_001008844.3:c.1045-30_1045-27delinsGCTA	NP_001008844.1:n.1045-30_1045-27delinsGCTA
NM_001319034.2:c.1045-30_1045-27delinsGCTA	NP_001305963.1:n.1045-30_1045-27delinsGCTA