Canonical Allele Identifier: CA716226845

Linked Data

dbSNP Id: rs1131445

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.81309441T>A , CM000677.2:g.81309441T>A GRCh38
NC_000015.9:g.81601782T>A , CM000677.1:g.81601782T>A GRCh37
NC_000015.8:g.79388837T>A NCBI36
NG_029933.1:g.117564T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000302987.10:c.*643T>A (IL16) ENSP00000302935.5:n.*643T>A
ENST00000706926.1:c.*643T>A (IL16) ENSP00000516648.1:n.*643T>A
ENST00000302987.9:c.*643T>A (IL16) ENSP00000302935.5:n.*643T>A
ENST00000683961.1:c.*643T>A (IL16) MANE Select ENSP00000508085.1:n.*643T>A
ENST00000302824.7:c.*3815A>T (STARD5) MANE Select ENSP00000304032.6:n.*3815A>T
ENST00000302824.6:c.*3815A>T (STARD5) ENSP00000304032.6:n.*3815A>T
ENST00000394660.6:c.*643T>A (IL16) ENSP00000378155.2:n.*643T>A
ENST00000560916.1:n.462A>T (STARD5)
NM_001172128.1:c.*643T>A (IL16) NP_001165599.1:n.*643T>A
NM_004513.5:c.*643T>A (IL16) NP_004504.3:n.*643T>A
NM_172217.3:c.*643T>A (IL16) NP_757366.2:n.*643T>A
NM_001352684.1:c.*643T>A (IL16) NP_001339613.1:n.*643T>A
NM_001352685.1:c.*643T>A (IL16) NP_001339614.1:n.*643T>A
NM_001352686.1:c.*643T>A (IL16) NP_001339615.1:n.*643T>A
NM_172217.4:c.*643T>A (IL16) NP_757366.2:n.*643T>A
NR_148035.1:n.4854T>A (IL16)
NM_181900.3:c.*3815A>T (STARD5) MANE Select NP_871629.1:n.*3815A>T
NM_001172128.2:c.*643T>A (IL16) NP_001165599.1:n.*643T>A
NM_001352684.2:c.*643T>A (IL16) NP_001339613.1:n.*643T>A
NM_001352685.2:c.*643T>A (IL16) NP_001339614.1:n.*643T>A
NM_004513.6:c.*643T>A (IL16) NP_004504.3:n.*643T>A
NM_172217.5:c.*643T>A (IL16) MANE Select NP_757366.2:n.*643T>A
NR_135013.2:n.4449A>T (STARD5)
NR_148035.2:n.4853T>A (IL16)
NM_001352686.2:c.*643T>A (IL16) NP_001339615.1:n.*643T>A