Canonical Allele Identifier: CA2683134192

Linked Data

gnomAD v4: 7-66995201-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.66995201G>T , CM000669.2:g.66995201G>T GRCh38
NC_000007.13:g.66460188G>T , CM000669.1:g.66460188G>T GRCh37
NC_000007.12:g.66097623G>T NCBI36
NG_007277.1:g.5401C>A , LRG_104:g.5401C>A
NG_033069.1:g.3397G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000414306.6:c.128+89C>A (SBDS) ENSP00000394586.1:n.128+89C>A
ENST00000697861.1:c.128+89C>A (SBDS) ENSP00000513460.1:n.128+89C>A
ENST00000697862.1:c.128+89C>A (SBDS) ENSP00000513461.1:n.128+89C>A
ENST00000697863.1:c.71+89C>A (SBDS) ENSP00000513462.1:n.71+89C>A
ENST00000697864.1:n.413C>A (SBDS)
ENST00000697865.1:c.71+89C>A (SBDS) ENSP00000513463.1:n.71+89C>A
ENST00000697866.1:c.-294C>A (SBDS) ENSP00000513464.1:n.-294C>A
ENST00000697868.1:c.128+89C>A (SBDS) ENSP00000513466.1:n.128+89C>A
ENST00000697869.1:c.128+89C>A (SBDS) ENSP00000513467.1:n.128+89C>A
ENST00000697897.1:c.128+89C>A (SBDS) ENSP00000513469.1:n.128+89C>A
ENST00000246868.7:c.128+89C>A (SBDS) MANE Select ENSP00000246868.2:n.128+89C>A
ENST00000246868.6:c.128+89C>A (SBDS) ENSP00000246868.2:n.128+89C>A
ENST00000414306.5:c.128+89C>A (SBDS) ENSP00000394586.1:n.128+89C>A
ENST00000490953.5:n.277+89C>A (SBDS)
ENST00000491969.5:n.29G>T (TYW1)
ENST00000617799.1:c.127+89C>A (SBDS) ENSP00000483040.1:n.127+89C>A
NM_016038.2:c.128+89C>A , LRG_104t1:c.128+89C>A (SBDS) NP_057122.2:n.128+89C>A
NM_016038.3:c.128+89C>A (SBDS) NP_057122.2:n.128+89C>A
NM_016038.4:c.128+89C>A (SBDS) MANE Select NP_057122.2:n.128+89C>A