Canonical Allele Identifier: CA34786281
Gene: BRINP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.190287960A>G , CM000663.2:g.190287960A>G GRCh38
NC_000001.10:g.190257090A>G , CM000663.1:g.190257090A>G GRCh37
NC_000001.9:g.188523713A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000367462.5:c.237-6210T>C MANE Select ENSP00000356432.3:n.237-6210T>C
ENST00000367462.4:c.237-6210T>C ENSP00000356432.3:n.237-6210T>C
ENST00000631494.1:c.237-6210T>C ENSP00000487601.1:n.237-6210T>C
NM_199051.1:c.237-6210T>C NP_950252.1:n.237-6210T>C
XM_005245117.1:c.237-6210T>C XP_005245174.1:n.237-6210T>C
XM_005245118.3:c.237-6210T>C XP_005245175.1:n.237-6210T>C
XM_005245120.2:c.237-6210T>C XP_005245177.1:n.237-6210T>C
XM_011509472.1:c.147-6210T>C XP_011507774.1:n.147-6210T>C
XM_011509473.1:c.147-6210T>C XP_011507775.1:n.147-6210T>C
XM_011509474.1:c.147-6210T>C XP_011507776.1:n.147-6210T>C
XM_011509475.1:c.108-6210T>C XP_011507777.1:n.108-6210T>C
XM_011509476.1:c.122-22905T>C XP_011507778.1:n.122-22905T>C
XR_922372.1:n.81+22921A>G
XR_922373.1:n.68+22921A>G
XR_922374.1:n.81+22921A>G
NM_001317188.1:c.122-22905T>C NP_001304117.1:n.122-22905T>C
NM_199051.2:c.237-6210T>C NP_950252.1:n.237-6210T>C
XM_011509472.2:c.147-6210T>C XP_011507774.1:n.147-6210T>C
XM_011509475.2:c.108-6210T>C XP_011507777.1:n.108-6210T>C
XM_011509476.2:c.122-22905T>C XP_011507778.1:n.122-22905T>C
XM_017001125.1:c.237-6210T>C XP_016856614.1:n.237-6210T>C
XM_017001126.1:c.237-6210T>C XP_016856615.1:n.237-6210T>C
XM_017001127.1:c.147-6210T>C XP_016856616.1:n.147-6210T>C
XM_017001128.1:c.147-6210T>C XP_016856617.1:n.147-6210T>C
XM_017001129.1:c.122-22905T>C XP_016856618.1:n.122-22905T>C
XM_017001130.1:c.122-22905T>C XP_016856619.1:n.122-22905T>C
XM_017001131.1:c.-643-6210T>C XP_016856620.1:n.-643-6210T>C
XM_017001132.1:c.237-6210T>C XP_016856621.1:n.237-6210T>C
XM_017001133.1:c.237-6210T>C XP_016856622.1:n.237-6210T>C
NM_199051.3:c.237-6210T>C MANE Select NP_950252.1:n.237-6210T>C
NM_001317188.2:c.122-22905T>C NP_001304117.1:n.122-22905T>C