Canonical Allele Identifier: CA2641387026

Gene: DSC2

Linked Data

• gnomAD v4: 18-31079769-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31079769A>G , CM000680.2:g.31079769A>G	GRCh38
NC_000018.9:g.28659735A>G , CM000680.1:g.28659735A>G	GRCh37
NC_000018.8:g.26913733A>G	NCBI36
NG_008208.2:g.27657T>C , LRG_400:g.27657T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682357.1:c.1234+78T>C	ENSP00000507826.1:n.1234+78T>C
ENST00000251081.8:c.1663+78T>C	ENSP00000251081.6:n.1663+78T>C
ENST00000280904.11:c.1663+78T>C MANE Select	ENSP00000280904.6:n.1663+78T>C
ENST00000648081.1:c.1234+78T>C	ENSP00000497441.1:n.1234+78T>C
ENST00000251081.6:c.1663+78T>C	ENSP00000251081.6:n.1663+78T>C
ENST00000280904.10:c.1663+78T>C	ENSP00000280904.6:n.1663+78T>C
NM_004949.4:c.1663+78T>C	NP_004940.1:n.1663+78T>C
NM_024422.4:c.1663+78T>C	NP_077740.1:n.1663+78T>C
XM_005258206.3:c.1234+78T>C	XP_005258263.1:n.1234+78T>C
XM_005258206.4:c.1234+78T>C	XP_005258263.1:n.1234+78T>C
NM_004949.5:c.1663+78T>C	NP_004940.1:n.1663+78T>C
NM_024422.6:c.1663+78T>C MANE Select	NP_077740.1:n.1663+78T>C