Canonical Allele Identifier: CA490009217

Gene: STARD9

Linked Data

• MyVariant Identifiers: chr15:g.42984189G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42691991G>C , CM000677.2:g.42691991G>C	GRCh38
NC_000015.9:g.42984189G>C , CM000677.1:g.42984189G>C	GRCh37
NC_000015.8:g.40771481G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000290607.12:c.10413G>C MANE Select	ENSP00000290607.7:p.Leu3471=
ENST00000290607.11:c.10413G>C	ENSP00000290607.7:p.Leu3471=
ENST00000562619.1:c.2397G>C	ENSP00000454648.1:p.Leu799=
NM_020759.2:c.10413G>C	NP_065810.2:p.Leu3471=
XM_011521831.1:c.10413G>C	XP_011520133.1:p.Leu3471=
XM_011521832.1:c.10410G>C	XP_011520134.1:p.Leu3470=
XM_011521833.1:c.10380G>C	XP_011520135.1:p.Leu3460=
XM_011521834.1:c.10350G>C	XP_011520136.1:p.Leu3450=
XM_011521835.1:c.10272G>C	XP_011520137.1:p.Leu3424=
XM_011521836.1:c.10251G>C	XP_011520138.1:p.Leu3417=
XM_011521837.1:c.10161G>C	XP_011520139.1:p.Leu3387=
XM_011521838.1:c.9699G>C	XP_011520140.1:p.Leu3233=
XM_011521839.1:c.7893G>C	XP_011520141.1:p.Leu2631=
XR_931874.1:n.10495G>C
XM_011521831.3:c.10413G>C	XP_011520133.1:p.Leu3471=
XM_011521832.2:c.10410G>C	XP_011520134.1:p.Leu3470=
XM_011521833.2:c.10380G>C	XP_011520135.1:p.Leu3460=
XM_011521834.3:c.10350G>C	XP_011520136.1:p.Leu3450=
XM_011521835.3:c.10272G>C	XP_011520137.1:p.Leu3424=
XM_011521836.2:c.10251G>C	XP_011520138.1:p.Leu3417=
XM_011521837.3:c.10161G>C	XP_011520139.1:p.Leu3387=
XM_011521839.3:c.7893G>C	XP_011520141.1:p.Leu2631=
XM_017022439.2:c.10335G>C	XP_016877928.1:p.Leu3445=
XM_017022440.1:c.10251G>C	XP_016877929.1:p.Leu3417=
XM_017022441.2:c.10194G>C	XP_016877930.1:p.Leu3398=
XM_017022442.1:c.9699G>C	XP_016877931.1:p.Leu3233=
XM_017022443.1:c.9699G>C	XP_016877932.1:p.Leu3233=
XR_931874.3:n.10519G>C
NM_020759.3:c.10413G>C MANE Select	NP_065810.2:p.Leu3471=