Canonical Allele Identifier: CA1608613681

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7585221T= , CM000668.2:g.7585221T=	GRCh38
NC_000006.11:g.7585454T= , CM000668.1:g.7585454T=	GRCh37
NC_000006.10:g.7530453T=	NCBI36
NG_008803.1:g.48585T= , LRG_423:g.48585T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.6630T=	ENSP00000518230.1:p.Ala2210=
ENST00000379802.8:c.7959T= MANE Select	ENSP00000369129.3:p.Ala2653=
ENST00000379802.7:c.7959T=	ENSP00000369129.3:p.Ala2653=
ENST00000418664.2:c.6162T=	ENSP00000396591.2:p.Ala2054=
NM_001008844.1:c.6162T=	NP_001008844.1:p.Ala2054=
NM_004415.2:c.7959T= , LRG_423t1:c.7959T=	NP_004406.2:p.Ala2653=
XM_011514323.1:c.6630T=	XP_011512625.1:p.Ala2210=
NM_001008844.2:c.6162T=	NP_001008844.1:p.Ala2054=
NM_001319034.1:c.6630T=	NP_001305963.1:p.Ala2210=
NM_004415.3:c.7959T=	NP_004406.2:p.Ala2653=
NM_004415.4:c.7959T= MANE Select	NP_004406.2:p.Ala2653=
NM_001008844.3:c.6162T=	NP_001008844.1:p.Ala2054=
NM_001319034.2:c.6630T=	NP_001305963.1:p.Ala2210=