Canonical Allele Identifier: CA272758513

Gene: STRA6

Linked Data

• dbSNP Id: rs775117127
• gnomAD v3: 15-74195253-G-C
• gnomAD v4: 15-74195253-G-C
• MyVariant Identifiers: chr15:g.74487594G>C (hg19) ; chr15:g.74195253G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74195253G>C , CM000677.2:g.74195253G>C	GRCh38
NC_000015.9:g.74487594G>C , CM000677.1:g.74487594G>C	GRCh37
NC_000015.8:g.72274647G>C	NCBI36
NG_009207.1:g.18778C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000395105.9:c.597+49C>G MANE Select	ENSP00000378537.4:n.597+49C>G
ENST00000323940.9:c.597+49C>G	ENSP00000326085.5:n.597+49C>G
ENST00000395105.8:c.597+49C>G	ENSP00000378537.4:n.597+49C>G
ENST00000416286.7:c.573+49C>G	ENSP00000400403.3:n.573+49C>G
ENST00000423167.6:c.570+49C>G	ENSP00000413012.2:n.570+49C>G
ENST00000432245.6:c.*349C>G	ENSP00000407176.2:n.*349C>G
ENST00000449139.6:c.597+49C>G	ENSP00000410221.2:n.597+49C>G
ENST00000535552.5:c.708+49C>G	ENSP00000440238.1:n.708+49C>G
ENST00000545137.5:n.306+399C>G
ENST00000563965.5:c.714+49C>G	ENSP00000456609.1:n.714+49C>G
ENST00000569936.5:c.597+49C>G	ENSP00000461799.1:n.597+49C>G
ENST00000574278.5:c.642+49C>G	ENSP00000458827.1:n.642+49C>G
ENST00000574439.5:n.869+49C>G
ENST00000616000.4:c.597+49C>G	ENSP00000479112.1:n.597+49C>G
NM_001142617.1:c.597+49C>G	NP_001136089.1:n.597+49C>G
NM_001142618.1:c.597+49C>G	NP_001136090.1:n.597+49C>G
NM_001142619.1:c.570+49C>G	NP_001136091.1:n.570+49C>G
NM_001142620.1:c.*349C>G	NP_001136092.1:n.*349C>G
NM_001199040.1:c.708+49C>G	NP_001185969.1:n.708+49C>G
NM_001199041.1:c.642+49C>G	NP_001185970.1:n.642+49C>G
NM_001199042.1:c.714+49C>G	NP_001185971.1:n.714+49C>G
NM_022369.3:c.597+49C>G	NP_071764.3:n.597+49C>G
XM_011521883.1:c.597+49C>G	XP_011520185.1:n.597+49C>G
XM_011521884.1:c.408+49C>G	XP_011520186.1:n.408+49C>G
XM_011521885.1:c.714+49C>G	XP_011520187.1:n.714+49C>G
XR_931877.1:n.720+49C>G
XM_011521885.2:c.714+49C>G	XP_011520187.1:n.714+49C>G
XM_017022478.1:c.645+49C>G	XP_016877967.1:n.645+49C>G
XM_017022479.1:c.597+49C>G	XP_016877968.1:n.597+49C>G
XM_017022480.1:c.408+49C>G	XP_016877969.1:n.408+49C>G
XR_931877.2:n.720+49C>G
NM_022369.4:c.597+49C>G MANE Select	NP_071764.3:n.597+49C>G
NM_001142617.2:c.597+49C>G	NP_001136089.1:n.597+49C>G
NM_001142619.2:c.570+49C>G	NP_001136091.1:n.570+49C>G
NM_001199042.2:c.714+49C>G	NP_001185971.1:n.714+49C>G
NM_001142618.2:c.597+49C>G	NP_001136090.1:n.597+49C>G
NM_001142620.2:c.*349C>G	NP_001136092.1:n.*349C>G
NM_001199040.2:c.708+49C>G	NP_001185969.1:n.708+49C>G
NM_001199041.2:c.642+49C>G	NP_001185970.1:n.642+49C>G