Canonical Allele Identifier: CA2629451626

Gene: STRA6

Linked Data

• gnomAD v4: 15-74180746-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74180746_74180747insC , CM000677.2:g.74180746_74180747insC	GRCh38
NC_000015.9:g.74473087_74473088insC , CM000677.1:g.74473087_74473088insC	GRCh37
NC_000015.8:g.72260140_72260141insC	NCBI36
NG_009207.1:g.33284_33285insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395105.9:c.1840+35_1840+36insG MANE Select	ENSP00000378537.4:n.1840+35_1840+36insG
ENST00000323940.9:c.1840+35_1840+36insG	ENSP00000326085.5:n.1840+35_1840+36insG
ENST00000395105.8:c.1840+35_1840+36insG	ENSP00000378537.4:n.1840+35_1840+36insG
ENST00000416286.7:c.1816+35_1816+36insG	ENSP00000400403.3:n.1816+35_1816+36insG
ENST00000423167.6:c.1813+35_1813+36insG	ENSP00000413012.2:n.1813+35_1813+36insG
ENST00000449139.6:c.1840+35_1840+36insG	ENSP00000410221.2:n.1840+35_1840+36insG
ENST00000535552.5:c.1951+35_1951+36insG	ENSP00000440238.1:n.1951+35_1951+36insG
ENST00000545137.5:n.1549+35_1549+36insG
ENST00000563965.5:c.1957+35_1957+36insG	ENSP00000456609.1:n.1957+35_1957+36insG
ENST00000572785.1:c.695+35_695+36insG
ENST00000574278.5:c.1885+35_1885+36insG	ENSP00000458827.1:n.1885+35_1885+36insG
ENST00000574439.5:n.2112+35_2112+36insG
ENST00000616000.4:c.1840+35_1840+36insG	ENSP00000479112.1:n.1840+35_1840+36insG
NM_001142617.1:c.1840+35_1840+36insG	NP_001136089.1:n.1840+35_1840+36insG
NM_001142618.1:c.1840+35_1840+36insG	NP_001136090.1:n.1840+35_1840+36insG
NM_001142619.1:c.1813+35_1813+36insG	NP_001136091.1:n.1813+35_1813+36insG
NM_001199040.1:c.1951+35_1951+36insG	NP_001185969.1:n.1951+35_1951+36insG
NM_001199041.1:c.1885+35_1885+36insG	NP_001185970.1:n.1885+35_1885+36insG
NM_001199042.1:c.1957+35_1957+36insG	NP_001185971.1:n.1957+35_1957+36insG
NM_022369.3:c.1840+35_1840+36insG	NP_071764.3:n.1840+35_1840+36insG
XM_011521883.1:c.1840+35_1840+36insG	XP_011520185.1:n.1840+35_1840+36insG
XM_011521884.1:c.1651+35_1651+36insG	XP_011520186.1:n.1651+35_1651+36insG
XM_017022478.1:c.1888+35_1888+36insG	XP_016877967.1:n.1888+35_1888+36insG
XM_017022479.1:c.1840+35_1840+36insG	XP_016877968.1:n.1840+35_1840+36insG
XM_017022480.1:c.1651+35_1651+36insG	XP_016877969.1:n.1651+35_1651+36insG
NM_022369.4:c.1840+35_1840+36insG MANE Select	NP_071764.3:n.1840+35_1840+36insG
NM_001142617.2:c.1840+35_1840+36insG	NP_001136089.1:n.1840+35_1840+36insG
NM_001142619.2:c.1813+35_1813+36insG	NP_001136091.1:n.1813+35_1813+36insG
NM_001199042.2:c.1957+35_1957+36insG	NP_001185971.1:n.1957+35_1957+36insG
NM_001142618.2:c.1840+35_1840+36insG	NP_001136090.1:n.1840+35_1840+36insG
NM_001199040.2:c.1951+35_1951+36insG	NP_001185969.1:n.1951+35_1951+36insG
NM_001199041.2:c.1885+35_1885+36insG	NP_001185970.1:n.1885+35_1885+36insG