Canonical Allele Identifier: CA10642544

Gene: STRA6

Linked Data

• ClinVar Variation Id: 317080
• ClinVar RCV Id: RCV000361025
• dbSNP Id: rs75117524
• gnomAD v2: 15-74471932-A-G
• gnomAD v3: 15-74179591-A-G
• gnomAD v4: 15-74179591-A-G
• MyVariant Identifiers: chr15:g.74471932A>G (hg19) ; chr15:g.74179591A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74179591A>G , CM000677.2:g.74179591A>G	GRCh38
NC_000015.9:g.74471932A>G , CM000677.1:g.74471932A>G	GRCh37
NC_000015.8:g.72258985A>G	NCBI36
NG_009207.1:g.34440T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000395105.9:c.*489T>C MANE Select	ENSP00000378537.4:n.*489T>C
ENST00000323940.9:c.*489T>C	ENSP00000326085.5:n.*489T>C
ENST00000395105.8:c.*489T>C	ENSP00000378537.4:n.*489T>C
ENST00000416286.7:c.*489T>C	ENSP00000400403.3:n.*489T>C
ENST00000423167.6:c.*489T>C	ENSP00000413012.2:n.*489T>C
ENST00000449139.6:c.*489T>C	ENSP00000410221.2:n.*489T>C
ENST00000545137.5:n.2202T>C
ENST00000574439.5:n.2765T>C
ENST00000616000.4:c.*489T>C	ENSP00000479112.1:n.*489T>C
NM_001142617.1:c.*489T>C	NP_001136089.1:n.*489T>C
NM_001142618.1:c.*489T>C	NP_001136090.1:n.*489T>C
NM_001142619.1:c.*489T>C	NP_001136091.1:n.*489T>C
NM_001199040.1:c.*489T>C	NP_001185969.1:n.*489T>C
NM_001199041.1:c.*489T>C	NP_001185970.1:n.*489T>C
NM_001199042.1:c.*489T>C	NP_001185971.1:n.*489T>C
NM_022369.3:c.*489T>C	NP_071764.3:n.*489T>C
XM_011521883.1:c.*489T>C	XP_011520185.1:n.*489T>C
XM_011521884.1:c.*489T>C	XP_011520186.1:n.*489T>C
XM_017022478.1:c.*489T>C	XP_016877967.1:n.*489T>C
XM_017022479.1:c.*489T>C	XP_016877968.1:n.*489T>C
XM_017022480.1:c.*489T>C	XP_016877969.1:n.*489T>C
NM_022369.4:c.*489T>C MANE Select	NP_071764.3:n.*489T>C
NM_001142617.2:c.*489T>C	NP_001136089.1:n.*489T>C
NM_001142619.2:c.*489T>C	NP_001136091.1:n.*489T>C
NM_001199042.2:c.*489T>C	NP_001185971.1:n.*489T>C
NM_001142618.2:c.*489T>C	NP_001136090.1:n.*489T>C
NM_001199040.2:c.*489T>C	NP_001185969.1:n.*489T>C
NM_001199041.2:c.*489T>C	NP_001185970.1:n.*489T>C