Canonical Allele Identifier: CA2641387034

Gene: DSC2

Linked Data

• gnomAD v4: 18-31079787-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31079787A>T , CM000680.2:g.31079787A>T	GRCh38
NC_000018.9:g.28659753A>T , CM000680.1:g.28659753A>T	GRCh37
NC_000018.8:g.26913751A>T	NCBI36
NG_008208.2:g.27639T>A , LRG_400:g.27639T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682357.1:c.1234+60T>A	ENSP00000507826.1:n.1234+60T>A
ENST00000251081.8:c.1663+60T>A	ENSP00000251081.6:n.1663+60T>A
ENST00000280904.11:c.1663+60T>A MANE Select	ENSP00000280904.6:n.1663+60T>A
ENST00000648081.1:c.1234+60T>A	ENSP00000497441.1:n.1234+60T>A
ENST00000251081.6:c.1663+60T>A	ENSP00000251081.6:n.1663+60T>A
ENST00000280904.10:c.1663+60T>A	ENSP00000280904.6:n.1663+60T>A
NM_004949.4:c.1663+60T>A	NP_004940.1:n.1663+60T>A
NM_024422.4:c.1663+60T>A	NP_077740.1:n.1663+60T>A
XM_005258206.3:c.1234+60T>A	XP_005258263.1:n.1234+60T>A
XM_005258206.4:c.1234+60T>A	XP_005258263.1:n.1234+60T>A
NM_004949.5:c.1663+60T>A	NP_004940.1:n.1663+60T>A
NM_024422.6:c.1663+60T>A MANE Select	NP_077740.1:n.1663+60T>A