Canonical Allele Identifier: CA1608616076

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7585818C= , CM000668.2:g.7585818C=	GRCh38
NC_000006.11:g.7586051C= , CM000668.1:g.7586051C=	GRCh37
NC_000006.10:g.7531050C=	NCBI36
NG_008803.1:g.49182C= , LRG_423:g.49182C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000710359.1:c.7227C=	ENSP00000518230.1:p.Ala2409=
ENST00000379802.8:c.8556C= MANE Select	ENSP00000369129.3:p.Ala2852=
ENST00000379802.7:c.8556C=	ENSP00000369129.3:p.Ala2852=
ENST00000418664.2:c.6759C=	ENSP00000396591.2:p.Ala2253=
NM_001008844.1:c.6759C=	NP_001008844.1:p.Ala2253=
NM_004415.2:c.8556C= , LRG_423t1:c.8556C=	NP_004406.2:p.Ala2852=
XM_011514323.1:c.7227C=	XP_011512625.1:p.Ala2409=
NM_001008844.2:c.6759C=	NP_001008844.1:p.Ala2253=
NM_001319034.1:c.7227C=	NP_001305963.1:p.Ala2409=
NM_004415.3:c.8556C=	NP_004406.2:p.Ala2852=
NM_004415.4:c.8556C= MANE Select	NP_004406.2:p.Ala2852=
NM_001008844.3:c.6759C=	NP_001008844.1:p.Ala2253=
NM_001319034.2:c.7227C=	NP_001305963.1:p.Ala2409=