Canonical Allele Identifier: CA392076574

Gene: STARD9

Linked Data

• MyVariant Identifiers: chr15:g.42984197G>C (hg19) ; chr15:g.42691999G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42691999G>C , CM000677.2:g.42691999G>C	GRCh38
NC_000015.9:g.42984197G>C , CM000677.1:g.42984197G>C	GRCh37
NC_000015.8:g.40771489G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000290607.12:c.10421G>C MANE Select	ENSP00000290607.7:p.Arg3474Pro
ENST00000290607.11:c.10421G>C	ENSP00000290607.7:p.Arg3474Pro
ENST00000562619.1:c.2405G>C	ENSP00000454648.1:p.Arg802Pro
NM_020759.2:c.10421G>C	NP_065810.2:p.Arg3474Pro
XM_011521831.1:c.10421G>C	XP_011520133.1:p.Arg3474Pro
XM_011521832.1:c.10418G>C	XP_011520134.1:p.Arg3473Pro
XM_011521833.1:c.10388G>C	XP_011520135.1:p.Arg3463Pro
XM_011521834.1:c.10358G>C	XP_011520136.1:p.Arg3453Pro
XM_011521835.1:c.10280G>C	XP_011520137.1:p.Arg3427Pro
XM_011521836.1:c.10259G>C	XP_011520138.1:p.Arg3420Pro
XM_011521837.1:c.10169G>C	XP_011520139.1:p.Arg3390Pro
XM_011521838.1:c.9707G>C	XP_011520140.1:p.Arg3236Pro
XM_011521839.1:c.7901G>C	XP_011520141.1:p.Arg2634Pro
XR_931874.1:n.10503G>C
XM_011521831.3:c.10421G>C	XP_011520133.1:p.Arg3474Pro
XM_011521832.2:c.10418G>C	XP_011520134.1:p.Arg3473Pro
XM_011521833.2:c.10388G>C	XP_011520135.1:p.Arg3463Pro
XM_011521834.3:c.10358G>C	XP_011520136.1:p.Arg3453Pro
XM_011521835.3:c.10280G>C	XP_011520137.1:p.Arg3427Pro
XM_011521836.2:c.10259G>C	XP_011520138.1:p.Arg3420Pro
XM_011521837.3:c.10169G>C	XP_011520139.1:p.Arg3390Pro
XM_011521839.3:c.7901G>C	XP_011520141.1:p.Arg2634Pro
XM_017022439.2:c.10343G>C	XP_016877928.1:p.Arg3448Pro
XM_017022440.1:c.10259G>C	XP_016877929.1:p.Arg3420Pro
XM_017022441.2:c.10202G>C	XP_016877930.1:p.Arg3401Pro
XM_017022442.1:c.9707G>C	XP_016877931.1:p.Arg3236Pro
XM_017022443.1:c.9707G>C	XP_016877932.1:p.Arg3236Pro
XR_931874.3:n.10527G>C
NM_020759.3:c.10421G>C MANE Select	NP_065810.2:p.Arg3474Pro