Canonical Allele Identifier: CA2629451289

Gene: STRA6

Linked Data

• gnomAD v4: 15-74190777-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74190777C>G , CM000677.2:g.74190777C>G	GRCh38
NC_000015.9:g.74483118C>G , CM000677.1:g.74483118C>G	GRCh37
NC_000015.8:g.72270171C>G	NCBI36
NG_009207.1:g.23254G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000395105.9:c.927+63G>C MANE Select	ENSP00000378537.4:n.927+63G>C
ENST00000323940.9:c.927+63G>C	ENSP00000326085.5:n.927+63G>C
ENST00000395105.8:c.927+63G>C	ENSP00000378537.4:n.927+63G>C
ENST00000416286.7:c.903+63G>C	ENSP00000400403.3:n.903+63G>C
ENST00000423167.6:c.900+63G>C	ENSP00000413012.2:n.900+63G>C
ENST00000449139.6:c.927+63G>C	ENSP00000410221.2:n.927+63G>C
ENST00000535552.5:c.1038+63G>C	ENSP00000440238.1:n.1038+63G>C
ENST00000545137.5:n.636+63G>C
ENST00000563965.5:c.1044+63G>C	ENSP00000456609.1:n.1044+63G>C
ENST00000569936.5:c.1057+63G>C	ENSP00000461799.1:n.1057+63G>C
ENST00000574278.5:c.972+63G>C	ENSP00000458827.1:n.972+63G>C
ENST00000574439.5:n.1199+63G>C
ENST00000616000.4:c.927+63G>C	ENSP00000479112.1:n.927+63G>C
NM_001142617.1:c.927+63G>C	NP_001136089.1:n.927+63G>C
NM_001142618.1:c.927+63G>C	NP_001136090.1:n.927+63G>C
NM_001142619.1:c.900+63G>C	NP_001136091.1:n.900+63G>C
NM_001199040.1:c.1038+63G>C	NP_001185969.1:n.1038+63G>C
NM_001199041.1:c.972+63G>C	NP_001185970.1:n.972+63G>C
NM_001199042.1:c.1044+63G>C	NP_001185971.1:n.1044+63G>C
NM_022369.3:c.927+63G>C	NP_071764.3:n.927+63G>C
XM_011521883.1:c.927+63G>C	XP_011520185.1:n.927+63G>C
XM_011521884.1:c.738+63G>C	XP_011520186.1:n.738+63G>C
XM_011521885.1:c.1044+63G>C	XP_011520187.1:n.1044+63G>C
XR_931877.1:n.1050+63G>C
XM_011521885.2:c.1044+63G>C	XP_011520187.1:n.1044+63G>C
XM_017022478.1:c.975+63G>C	XP_016877967.1:n.975+63G>C
XM_017022479.1:c.927+63G>C	XP_016877968.1:n.927+63G>C
XM_017022480.1:c.738+63G>C	XP_016877969.1:n.738+63G>C
XR_931877.2:n.1050+63G>C
NM_022369.4:c.927+63G>C MANE Select	NP_071764.3:n.927+63G>C
NM_001142617.2:c.927+63G>C	NP_001136089.1:n.927+63G>C
NM_001142619.2:c.900+63G>C	NP_001136091.1:n.900+63G>C
NM_001199042.2:c.1044+63G>C	NP_001185971.1:n.1044+63G>C
NM_001142618.2:c.927+63G>C	NP_001136090.1:n.927+63G>C
NM_001199040.2:c.1038+63G>C	NP_001185969.1:n.1038+63G>C
NM_001199041.2:c.972+63G>C	NP_001185970.1:n.972+63G>C