Canonical Allele Identifier: CA448522104

Gene: DSP

Linked Data

• dbSNP Id: rs1758933933
• gnomAD v4: 6-7568556-T-C
• MyVariant Identifiers: chr6:g.7568789T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7568556T>C , CM000668.2:g.7568556T>C	GRCh38
NC_000006.11:g.7568789T>C , CM000668.1:g.7568789T>C	GRCh37
NC_000006.10:g.7513788T>C	NCBI36
NG_008803.1:g.31920T>C , LRG_423:g.31920T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000710359.1:c.1386T>C	ENSP00000518230.1:p.Ile462=
ENST00000379802.8:c.1386T>C MANE Select	ENSP00000369129.3:p.Ile462=
ENST00000379802.7:c.1386T>C	ENSP00000369129.3:p.Ile462=
ENST00000418664.2:c.1386T>C	ENSP00000396591.2:p.Ile462=
NM_001008844.1:c.1386T>C	NP_001008844.1:p.Ile462=
NM_004415.2:c.1386T>C , LRG_423t1:c.1386T>C	NP_004406.2:p.Ile462=
XM_011514323.1:c.1386T>C	XP_011512625.1:p.Ile462=
NM_001008844.2:c.1386T>C	NP_001008844.1:p.Ile462=
NM_001319034.1:c.1386T>C	NP_001305963.1:p.Ile462=
NM_004415.3:c.1386T>C	NP_004406.2:p.Ile462=
NM_004415.4:c.1386T>C MANE Select	NP_004406.2:p.Ile462=
NM_001008844.3:c.1386T>C	NP_001008844.1:p.Ile462=
NM_001319034.2:c.1386T>C	NP_001305963.1:p.Ile462=