Canonical Allele Identifier: CA2686929598
Gene: STAR HGNC NCBI

Linked Data

gnomAD v4: 8-38148533-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38148533C>A , CM000670.2:g.38148533C>A GRCh38
NC_000008.10:g.38006051C>A , CM000670.1:g.38006051C>A GRCh37
NC_000008.9:g.38125208C>A NCBI36
NG_011827.1:g.7550G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.178+108G>T MANE Select ENSP00000276449.3:n.178+108G>T
ENST00000276449.8:c.178+108G>T ENSP00000276449.3:n.178+108G>T
ENST00000520114.1:n.460G>T
ENST00000521236.1:c.-101+108G>T ENSP00000430030.1:n.-101+108G>T
ENST00000522050.1:c.114+108G>T
NM_000349.2:c.178+108G>T NP_000340.2:n.178+108G>T
XM_006716392.1:c.178+108G>T XP_006716455.1:n.178+108G>T
NM_000349.3:c.178+108G>T MANE Select NP_000340.2:n.178+108G>T