Canonical Allele Identifier: CA2293654827

Gene: DSC2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31089233A= , CM000680.2:g.31089233A=	GRCh38
NC_000018.9:g.28669196A= , CM000680.1:g.28669196A=	GRCh37
NC_000018.8:g.26923194A=	NCBI36
NG_008208.2:g.18193T= , LRG_400:g.18193T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682357.1:c.201+206T=	ENSP00000507826.1:n.201+206T=
ENST00000251081.8:c.630+206T=	ENSP00000251081.6:n.630+206T=
ENST00000280904.11:c.630+206T= MANE Select	ENSP00000280904.6:n.630+206T=
ENST00000648081.1:c.201+206T=	ENSP00000497441.1:n.201+206T=
ENST00000251081.6:c.630+206T=	ENSP00000251081.6:n.630+206T=
ENST00000280904.10:c.630+206T=	ENSP00000280904.6:n.630+206T=
NM_004949.4:c.630+206T=	NP_004940.1:n.630+206T=
NM_024422.4:c.630+206T=	NP_077740.1:n.630+206T=
XM_005258206.3:c.201+206T=	XP_005258263.1:n.201+206T=
XM_005258206.4:c.201+206T=	XP_005258263.1:n.201+206T=
NM_004949.5:c.630+206T=	NP_004940.1:n.630+206T=
NM_024422.6:c.630+206T= MANE Select	NP_077740.1:n.630+206T=