Canonical Allele Identifier: CA448517970

Gene: DSP

Linked Data

• MyVariant Identifiers: chr6:g.7565639C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7565406C>A , CM000668.2:g.7565406C>A	GRCh38
NC_000006.11:g.7565639C>A , CM000668.1:g.7565639C>A	GRCh37
NC_000006.10:g.7510638C>A	NCBI36
NG_008803.1:g.28770C>A , LRG_423:g.28770C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.825C>A	ENSP00000518230.1:p.Ile275=
ENST00000682228.1:n.149C>A
ENST00000379802.8:c.825C>A MANE Select	ENSP00000369129.3:p.Ile275=
ENST00000379802.7:c.825C>A	ENSP00000369129.3:p.Ile275=
ENST00000418664.2:c.825C>A	ENSP00000396591.2:p.Ile275=
ENST00000506617.1:n.343C>A
NM_001008844.1:c.825C>A	NP_001008844.1:p.Ile275=
NM_004415.2:c.825C>A , LRG_423t1:c.825C>A	NP_004406.2:p.Ile275=
XM_011514323.1:c.825C>A	XP_011512625.1:p.Ile275=
NM_001008844.2:c.825C>A	NP_001008844.1:p.Ile275=
NM_001319034.1:c.825C>A	NP_001305963.1:p.Ile275=
NM_004415.3:c.825C>A	NP_004406.2:p.Ile275=
NM_004415.4:c.825C>A MANE Select	NP_004406.2:p.Ile275=
NM_001008844.3:c.825C>A	NP_001008844.1:p.Ile275=
NM_001319034.2:c.825C>A	NP_001305963.1:p.Ile275=