Canonical Allele Identifier: CA460375148
Gene: STAR HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.38006202A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38148684A>T , CM000670.2:g.38148684A>T GRCh38
NC_000008.10:g.38006202A>T , CM000670.1:g.38006202A>T GRCh37
NC_000008.9:g.38125359A>T NCBI36
NG_011827.1:g.7399T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000276449.9:c.135T>A MANE Select ENSP00000276449.3:p.Pro45=
ENST00000276449.8:c.135T>A ENSP00000276449.3:p.Pro45=
ENST00000520114.1:n.309T>A
ENST00000521236.1:c.-144T>A ENSP00000430030.1:n.-144T>A
ENST00000522050.1:c.71T>A
NM_000349.2:c.135T>A NP_000340.2:p.Pro45=
XM_006716392.1:c.135T>A XP_006716455.1:p.Pro45=
NM_000349.3:c.135T>A MANE Select NP_000340.2:p.Pro45=