Canonical Allele Identifier: CA448716131

Gene: DSP

Linked Data

• MyVariant Identifiers: chr6:g.7583819A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7583586A>T , CM000668.2:g.7583586A>T	GRCh38
NC_000006.11:g.7583819A>T , CM000668.1:g.7583819A>T	GRCh37
NC_000006.10:g.7528818A>T	NCBI36
NG_008803.1:g.46950A>T , LRG_423:g.46950A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000710359.1:c.4995A>T	ENSP00000518230.1:p.Ser1665=
ENST00000379802.8:c.6324A>T MANE Select	ENSP00000369129.3:p.Ser2108=
ENST00000379802.7:c.6324A>T	ENSP00000369129.3:p.Ser2108=
ENST00000418664.2:c.4527A>T	ENSP00000396591.2:p.Ser1509=
NM_001008844.1:c.4527A>T	NP_001008844.1:p.Ser1509=
NM_004415.2:c.6324A>T , LRG_423t1:c.6324A>T	NP_004406.2:p.Ser2108=
XM_011514323.1:c.4995A>T	XP_011512625.1:p.Ser1665=
NM_001008844.2:c.4527A>T	NP_001008844.1:p.Ser1509=
NM_001319034.1:c.4995A>T	NP_001305963.1:p.Ser1665=
NM_004415.3:c.6324A>T	NP_004406.2:p.Ser2108=
NM_004415.4:c.6324A>T MANE Select	NP_004406.2:p.Ser2108=
NM_001008844.3:c.4527A>T	NP_001008844.1:p.Ser1509=
NM_001319034.2:c.4995A>T	NP_001305963.1:p.Ser1665=