Canonical Allele Identifier: CA14989081
Community Standard Title: NM_014351.4(SULT4A1):c.169+7524T>C
Gene: SULT4A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43854690A>G , CM000684.2:g.43854690A>G GRCh38
NC_000022.10:g.44250570A>G , CM000684.1:g.44250570A>G GRCh37
NC_000022.9:g.42581903A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_014351.4:c.169+7524T>C MANE Select NP_055166.1:n.169+7524T>C
ENST00000330884.9:c.169+7524T>C MANE Select ENSP00000332565.4:n.169+7524T>C
NM_014351.3:c.169+7524T>C NP_055166.1:n.169+7524T>C
ENST00000330884.8:c.169+7524T>C ENSP00000332565.4:n.169+7524T>C
ENST00000422525.1:c.169+7524T>C ENSP00000388285.1:n.169+7524T>C
ENST00000432404.5:c.169+7524T>C ENSP00000414220.1:n.169+7524T>C
XM_011530120.1:c.169+7524T>C XP_011528422.1:n.169+7524T>C
XM_011530120.3:c.169+7524T>C XP_011528422.1:n.169+7524T>C
XM_011530121.1:c.169+7524T>C XP_011528423.1:n.169+7524T>C
XR_001755207.1:n.219+7524T>C
XR_937838.1:n.219+7524T>C
XR_937838.2:n.219+7524T>C
XR_937839.1:n.219+7524T>C
XR_937839.3:n.221+7524T>C