Canonical Allele Identifier: CA392076524

Gene: STARD9

Linked Data

• MyVariant Identifiers: chr15:g.42984190C>A (hg19) ; chr15:g.42691992C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42691992C>A , CM000677.2:g.42691992C>A	GRCh38
NC_000015.9:g.42984190C>A , CM000677.1:g.42984190C>A	GRCh37
NC_000015.8:g.40771482C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000290607.12:c.10414C>A MANE Select	ENSP00000290607.7:p.Pro3472Thr
ENST00000290607.11:c.10414C>A	ENSP00000290607.7:p.Pro3472Thr
ENST00000562619.1:c.2398C>A	ENSP00000454648.1:p.Pro800Thr
NM_020759.2:c.10414C>A	NP_065810.2:p.Pro3472Thr
XM_011521831.1:c.10414C>A	XP_011520133.1:p.Pro3472Thr
XM_011521832.1:c.10411C>A	XP_011520134.1:p.Pro3471Thr
XM_011521833.1:c.10381C>A	XP_011520135.1:p.Pro3461Thr
XM_011521834.1:c.10351C>A	XP_011520136.1:p.Pro3451Thr
XM_011521835.1:c.10273C>A	XP_011520137.1:p.Pro3425Thr
XM_011521836.1:c.10252C>A	XP_011520138.1:p.Pro3418Thr
XM_011521837.1:c.10162C>A	XP_011520139.1:p.Pro3388Thr
XM_011521838.1:c.9700C>A	XP_011520140.1:p.Pro3234Thr
XM_011521839.1:c.7894C>A	XP_011520141.1:p.Pro2632Thr
XR_931874.1:n.10496C>A
XM_011521831.3:c.10414C>A	XP_011520133.1:p.Pro3472Thr
XM_011521832.2:c.10411C>A	XP_011520134.1:p.Pro3471Thr
XM_011521833.2:c.10381C>A	XP_011520135.1:p.Pro3461Thr
XM_011521834.3:c.10351C>A	XP_011520136.1:p.Pro3451Thr
XM_011521835.3:c.10273C>A	XP_011520137.1:p.Pro3425Thr
XM_011521836.2:c.10252C>A	XP_011520138.1:p.Pro3418Thr
XM_011521837.3:c.10162C>A	XP_011520139.1:p.Pro3388Thr
XM_011521839.3:c.7894C>A	XP_011520141.1:p.Pro2632Thr
XM_017022439.2:c.10336C>A	XP_016877928.1:p.Pro3446Thr
XM_017022440.1:c.10252C>A	XP_016877929.1:p.Pro3418Thr
XM_017022441.2:c.10195C>A	XP_016877930.1:p.Pro3399Thr
XM_017022442.1:c.9700C>A	XP_016877931.1:p.Pro3234Thr
XM_017022443.1:c.9700C>A	XP_016877932.1:p.Pro3234Thr
XR_931874.3:n.10520C>A
NM_020759.3:c.10414C>A MANE Select	NP_065810.2:p.Pro3472Thr