Canonical Allele Identifier: CA651386108

Gene: SBDS TYW1

Linked Data

• gnomAD v4: 7-66995187-C-A
• COSMIC: COSN14843425

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66995187C>A , CM000669.2:g.66995187C>A	GRCh38
NC_000007.13:g.66460174C>A , CM000669.1:g.66460174C>A	GRCh37
NC_000007.12:g.66097609C>A	NCBI36
NG_007277.1:g.5415G>T , LRG_104:g.5415G>T
NG_033069.1:g.3383C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000414306.6:c.128+103G>T (SBDS)	ENSP00000394586.1:n.128+103G>T
ENST00000697861.1:c.128+103G>T (SBDS)	ENSP00000513460.1:n.128+103G>T
ENST00000697862.1:c.128+103G>T (SBDS)	ENSP00000513461.1:n.128+103G>T
ENST00000697863.1:c.71+103G>T (SBDS)	ENSP00000513462.1:n.71+103G>T
ENST00000697864.1:n.427G>T (SBDS)
ENST00000697865.1:c.71+103G>T (SBDS)	ENSP00000513463.1:n.71+103G>T
ENST00000697866.1:c.-280G>T (SBDS)	ENSP00000513464.1:n.-280G>T
ENST00000697868.1:c.128+103G>T (SBDS)	ENSP00000513466.1:n.128+103G>T
ENST00000697869.1:c.128+103G>T (SBDS)	ENSP00000513467.1:n.128+103G>T
ENST00000697897.1:c.128+103G>T (SBDS)	ENSP00000513469.1:n.128+103G>T
ENST00000246868.7:c.128+103G>T (SBDS) MANE Select	ENSP00000246868.2:n.128+103G>T
ENST00000246868.6:c.128+103G>T (SBDS)	ENSP00000246868.2:n.128+103G>T
ENST00000414306.5:c.128+103G>T (SBDS)	ENSP00000394586.1:n.128+103G>T
ENST00000490953.5:n.277+103G>T (SBDS)
ENST00000491969.5:n.15C>A (TYW1)
ENST00000617799.1:c.127+103G>T (SBDS)	ENSP00000483040.1:n.127+103G>T
NM_016038.2:c.128+103G>T , LRG_104t1:c.128+103G>T (SBDS)	NP_057122.2:n.128+103G>T
NM_016038.3:c.128+103G>T (SBDS)	NP_057122.2:n.128+103G>T
NM_016038.4:c.128+103G>T (SBDS) MANE Select	NP_057122.2:n.128+103G>T