Canonical Allele Identifier: CA1608613691

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7585224G= , CM000668.2:g.7585224G=	GRCh38
NC_000006.11:g.7585457G= , CM000668.1:g.7585457G=	GRCh37
NC_000006.10:g.7530456G=	NCBI36
NG_008803.1:g.48588G= , LRG_423:g.48588G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.6633G=	ENSP00000518230.1:p.Gln2211=
ENST00000379802.8:c.7962G= MANE Select	ENSP00000369129.3:p.Gln2654=
ENST00000379802.7:c.7962G=	ENSP00000369129.3:p.Gln2654=
ENST00000418664.2:c.6165G=	ENSP00000396591.2:p.Gln2055=
NM_001008844.1:c.6165G=	NP_001008844.1:p.Gln2055=
NM_004415.2:c.7962G= , LRG_423t1:c.7962G=	NP_004406.2:p.Gln2654=
XM_011514323.1:c.6633G=	XP_011512625.1:p.Gln2211=
NM_001008844.2:c.6165G=	NP_001008844.1:p.Gln2055=
NM_001319034.1:c.6633G=	NP_001305963.1:p.Gln2211=
NM_004415.3:c.7962G=	NP_004406.2:p.Gln2654=
NM_004415.4:c.7962G= MANE Select	NP_004406.2:p.Gln2654=
NM_001008844.3:c.6165G=	NP_001008844.1:p.Gln2055=
NM_001319034.2:c.6633G=	NP_001305963.1:p.Gln2211=