Canonical Allele Identifier: CA402110552

Gene: DSC2

Linked Data

• MyVariant Identifiers: chr18:g.28662939T>A (hg19) ; chr18:g.31082973T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31082973T>A , CM000680.2:g.31082973T>A	GRCh38
NC_000018.9:g.28662939T>A , CM000680.1:g.28662939T>A	GRCh37
NC_000018.8:g.26916937T>A	NCBI36
NG_008208.2:g.24453A>T , LRG_400:g.24453A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682357.1:c.601A>T	ENSP00000507826.1:p.Asn201Tyr
ENST00000251081.8:c.1030A>T	ENSP00000251081.6:p.Asn344Tyr
ENST00000280904.11:c.1030A>T MANE Select	ENSP00000280904.6:p.Asn344Tyr
ENST00000648081.1:c.601A>T	ENSP00000497441.1:p.Asn201Tyr
ENST00000251081.6:c.1030A>T	ENSP00000251081.6:p.Asn344Tyr
ENST00000280904.10:c.1030A>T	ENSP00000280904.6:p.Asn344Tyr
NM_004949.4:c.1030A>T	NP_004940.1:p.Asn344Tyr
NM_024422.4:c.1030A>T	NP_077740.1:p.Asn344Tyr
XM_005258206.3:c.601A>T	XP_005258263.1:p.Asn201Tyr
XM_005258206.4:c.601A>T	XP_005258263.1:p.Asn201Tyr
NM_004949.5:c.1030A>T	NP_004940.1:p.Asn344Tyr
NM_024422.6:c.1030A>T MANE Select	NP_077740.1:p.Asn344Tyr