Canonical Allele Identifier: CA1608620560

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7567364_7567370delinsACACTCT , CM000668.2:g.7567364_7567370delinsACACTCT	GRCh38
NC_000006.11:g.7567597_7567603delinsACACTCT , CM000668.1:g.7567597_7567603delinsACACTCT	GRCh37
NC_000006.10:g.7512596_7512602delinsACACTCT	NCBI36
NG_008803.1:g.30728_30734delinsACACTCT , LRG_423:g.30728_30734delinsACACTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.1055_1061delinsACACTCT	ENSP00000518230.1:p.Asp352=
ENST00000682228.1:n.379_385delinsACACTCT
ENST00000379802.8:c.1055_1061delinsACACTCT MANE Select	ENSP00000369129.3:p.Asp352=
ENST00000379802.7:c.1055_1061delinsACACTCT	ENSP00000369129.3:p.Asp352=
ENST00000418664.2:c.1055_1061delinsACACTCT	ENSP00000396591.2:p.Asp352=
NM_001008844.1:c.1055_1061delinsACACTCT	NP_001008844.1:p.Asp352=
NM_004415.2:c.1055_1061delinsACACTCT , LRG_423t1:c.1055_1061delinsACACTCT	NP_004406.2:p.Asp352=
XM_011514323.1:c.1055_1061delinsACACTCT	XP_011512625.1:p.Asp352=
NM_001008844.2:c.1055_1061delinsACACTCT	NP_001008844.1:p.Asp352=
NM_001319034.1:c.1055_1061delinsACACTCT	NP_001305963.1:p.Asp352=
NM_004415.3:c.1055_1061delinsACACTCT	NP_004406.2:p.Asp352=
NM_004415.4:c.1055_1061delinsACACTCT MANE Select	NP_004406.2:p.Asp352=
NM_001008844.3:c.1055_1061delinsACACTCT	NP_001008844.1:p.Asp352=
NM_001319034.2:c.1055_1061delinsACACTCT	NP_001305963.1:p.Asp352=