Canonical Allele Identifier: CA14163144
Gene: STRA6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74208389C>T , CM000677.2:g.74208389C>T GRCh38
NC_000015.9:g.74500730C>T , CM000677.1:g.74500730C>T GRCh37
NC_000015.8:g.72287783C>T NCBI36
NG_009207.1:g.5642G>A
NG_054754.1:g.10685C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001142617.1:c.-16+411G>A NP_001136089.1:n.-16+411G>A
NM_001142617.2:c.-16+411G>A NP_001136089.1:n.-16+411G>A
NM_001142619.1:c.-16+411G>A NP_001136091.1:n.-16+411G>A
NM_001142619.2:c.-16+411G>A NP_001136091.1:n.-16+411G>A
NM_001142620.1:c.-16+411G>A NP_001136092.1:n.-16+411G>A
NM_001142620.2:c.-16+411G>A NP_001136092.1:n.-16+411G>A
NM_001199040.1:c.96+970G>A NP_001185969.1:n.96+970G>A
NM_001199040.2:c.96+970G>A NP_001185969.1:n.96+970G>A
ENST00000323940.9:c.-16+411G>A ENSP00000326085.5:n.-16+411G>A
ENST00000416286.7:c.-16+3738G>A ENSP00000400403.3:n.-16+3738G>A
ENST00000423167.6:c.-16+411G>A ENSP00000413012.2:n.-16+411G>A
ENST00000432245.6:c.-16+411G>A ENSP00000407176.2:n.-16+411G>A
ENST00000449139.6:c.-16+3738G>A ENSP00000410221.2:n.-16+3738G>A
ENST00000535552.5:c.96+970G>A ENSP00000440238.1:n.96+970G>A
ENST00000558645.5:n.90-999C>T
ENST00000560148.5:n.395-999C>T
ENST00000561332.1:n.50-999C>T
XM_011521883.1:c.-16+3738G>A XP_011520185.1:n.-16+3738G>A
XM_017022479.1:c.-48+3738G>A XP_016877968.1:n.-48+3738G>A