Canonical Allele Identifier: CA1608613364

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7585132_7585134delinsGAC , CM000668.2:g.7585132_7585134delinsGAC	GRCh38
NC_000006.11:g.7585365_7585367delinsGAC , CM000668.1:g.7585365_7585367delinsGAC	GRCh37
NC_000006.10:g.7530364_7530366delinsGAC	NCBI36
NG_008803.1:g.48496_48498delinsGAC , LRG_423:g.48496_48498delinsGAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.6541_6543delinsGAC	ENSP00000518230.1:p.Asp2181=
ENST00000379802.8:c.7870_7872delinsGAC MANE Select	ENSP00000369129.3:p.Asp2624=
ENST00000379802.7:c.7870_7872delinsGAC	ENSP00000369129.3:p.Asp2624=
ENST00000418664.2:c.6073_6075delinsGAC	ENSP00000396591.2:p.Asp2025=
NM_001008844.1:c.6073_6075delinsGAC	NP_001008844.1:p.Asp2025=
NM_004415.2:c.7870_7872delinsGAC , LRG_423t1:c.7870_7872delinsGAC	NP_004406.2:p.Asp2624=
XM_011514323.1:c.6541_6543delinsGAC	XP_011512625.1:p.Asp2181=
NM_001008844.2:c.6073_6075delinsGAC	NP_001008844.1:p.Asp2025=
NM_001319034.1:c.6541_6543delinsGAC	NP_001305963.1:p.Asp2181=
NM_004415.3:c.7870_7872delinsGAC	NP_004406.2:p.Asp2624=
NM_004415.4:c.7870_7872delinsGAC MANE Select	NP_004406.2:p.Asp2624=
NM_001008844.3:c.6073_6075delinsGAC	NP_001008844.1:p.Asp2025=
NM_001319034.2:c.6541_6543delinsGAC	NP_001305963.1:p.Asp2181=