Canonical Allele Identifier: CA272745758

Gene: STRA6

Linked Data

• dbSNP Id: rs980422950
• gnomAD v3: 15-74179607-T-C
• gnomAD v4: 15-74179607-T-C
• MyVariant Identifiers: chr15:g.74471948T>C (hg19) ; chr15:g.74179607T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74179607T>C , CM000677.2:g.74179607T>C	GRCh38
NC_000015.9:g.74471948T>C , CM000677.1:g.74471948T>C	GRCh37
NC_000015.8:g.72259001T>C	NCBI36
NG_009207.1:g.34424A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000395105.9:c.*473A>G MANE Select	ENSP00000378537.4:n.*473A>G
ENST00000323940.9:c.*473A>G	ENSP00000326085.5:n.*473A>G
ENST00000395105.8:c.*473A>G	ENSP00000378537.4:n.*473A>G
ENST00000416286.7:c.*473A>G	ENSP00000400403.3:n.*473A>G
ENST00000423167.6:c.*473A>G	ENSP00000413012.2:n.*473A>G
ENST00000449139.6:c.*473A>G	ENSP00000410221.2:n.*473A>G
ENST00000545137.5:n.2186A>G
ENST00000574439.5:n.2749A>G
ENST00000616000.4:c.*473A>G	ENSP00000479112.1:n.*473A>G
NM_001142617.1:c.*473A>G	NP_001136089.1:n.*473A>G
NM_001142618.1:c.*473A>G	NP_001136090.1:n.*473A>G
NM_001142619.1:c.*473A>G	NP_001136091.1:n.*473A>G
NM_001199040.1:c.*473A>G	NP_001185969.1:n.*473A>G
NM_001199041.1:c.*473A>G	NP_001185970.1:n.*473A>G
NM_001199042.1:c.*473A>G	NP_001185971.1:n.*473A>G
NM_022369.3:c.*473A>G	NP_071764.3:n.*473A>G
XM_011521883.1:c.*473A>G	XP_011520185.1:n.*473A>G
XM_011521884.1:c.*473A>G	XP_011520186.1:n.*473A>G
XM_017022478.1:c.*473A>G	XP_016877967.1:n.*473A>G
XM_017022479.1:c.*473A>G	XP_016877968.1:n.*473A>G
XM_017022480.1:c.*473A>G	XP_016877969.1:n.*473A>G
NM_022369.4:c.*473A>G MANE Select	NP_071764.3:n.*473A>G
NM_001142617.2:c.*473A>G	NP_001136089.1:n.*473A>G
NM_001142619.2:c.*473A>G	NP_001136091.1:n.*473A>G
NM_001199042.2:c.*473A>G	NP_001185971.1:n.*473A>G
NM_001142618.2:c.*473A>G	NP_001136090.1:n.*473A>G
NM_001199040.2:c.*473A>G	NP_001185969.1:n.*473A>G
NM_001199041.2:c.*473A>G	NP_001185970.1:n.*473A>G