Canonical Allele Identifier: CA619411522

Gene: STRA6

Linked Data

• dbSNP Id: rs1364830055
• gnomAD v2: 15-74487592-T-C
• gnomAD v4: 15-74195251-T-C
• MyVariant Identifiers: chr15:g.74487592T>C (hg19) ; chr15:g.74195251T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74195251T>C , CM000677.2:g.74195251T>C	GRCh38
NC_000015.9:g.74487592T>C , CM000677.1:g.74487592T>C	GRCh37
NC_000015.8:g.72274645T>C	NCBI36
NG_009207.1:g.18780A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000395105.9:c.597+51A>G MANE Select	ENSP00000378537.4:n.597+51A>G
ENST00000323940.9:c.597+51A>G	ENSP00000326085.5:n.597+51A>G
ENST00000395105.8:c.597+51A>G	ENSP00000378537.4:n.597+51A>G
ENST00000416286.7:c.573+51A>G	ENSP00000400403.3:n.573+51A>G
ENST00000423167.6:c.570+51A>G	ENSP00000413012.2:n.570+51A>G
ENST00000432245.6:c.*351A>G	ENSP00000407176.2:n.*351A>G
ENST00000449139.6:c.597+51A>G	ENSP00000410221.2:n.597+51A>G
ENST00000535552.5:c.708+51A>G	ENSP00000440238.1:n.708+51A>G
ENST00000545137.5:n.306+401A>G
ENST00000563965.5:c.714+51A>G	ENSP00000456609.1:n.714+51A>G
ENST00000569936.5:c.597+51A>G	ENSP00000461799.1:n.597+51A>G
ENST00000574278.5:c.642+51A>G	ENSP00000458827.1:n.642+51A>G
ENST00000574439.5:n.869+51A>G
ENST00000616000.4:c.597+51A>G	ENSP00000479112.1:n.597+51A>G
NM_001142617.1:c.597+51A>G	NP_001136089.1:n.597+51A>G
NM_001142618.1:c.597+51A>G	NP_001136090.1:n.597+51A>G
NM_001142619.1:c.570+51A>G	NP_001136091.1:n.570+51A>G
NM_001142620.1:c.*351A>G	NP_001136092.1:n.*351A>G
NM_001199040.1:c.708+51A>G	NP_001185969.1:n.708+51A>G
NM_001199041.1:c.642+51A>G	NP_001185970.1:n.642+51A>G
NM_001199042.1:c.714+51A>G	NP_001185971.1:n.714+51A>G
NM_022369.3:c.597+51A>G	NP_071764.3:n.597+51A>G
XM_011521883.1:c.597+51A>G	XP_011520185.1:n.597+51A>G
XM_011521884.1:c.408+51A>G	XP_011520186.1:n.408+51A>G
XM_011521885.1:c.714+51A>G	XP_011520187.1:n.714+51A>G
XR_931877.1:n.720+51A>G
XM_011521885.2:c.714+51A>G	XP_011520187.1:n.714+51A>G
XM_017022478.1:c.645+51A>G	XP_016877967.1:n.645+51A>G
XM_017022479.1:c.597+51A>G	XP_016877968.1:n.597+51A>G
XM_017022480.1:c.408+51A>G	XP_016877969.1:n.408+51A>G
XR_931877.2:n.720+51A>G
NM_022369.4:c.597+51A>G MANE Select	NP_071764.3:n.597+51A>G
NM_001142617.2:c.597+51A>G	NP_001136089.1:n.597+51A>G
NM_001142619.2:c.570+51A>G	NP_001136091.1:n.570+51A>G
NM_001199042.2:c.714+51A>G	NP_001185971.1:n.714+51A>G
NM_001142618.2:c.597+51A>G	NP_001136090.1:n.597+51A>G
NM_001142620.2:c.*351A>G	NP_001136092.1:n.*351A>G
NM_001199040.2:c.708+51A>G	NP_001185969.1:n.708+51A>G
NM_001199041.2:c.642+51A>G	NP_001185970.1:n.642+51A>G