Canonical Allele Identifier: CA10746758

Gene: BRINP3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.190337212A>G , CM000663.2:g.190337212A>G	GRCh38
NC_000001.10:g.190306342A>G , CM000663.1:g.190306342A>G	GRCh37
NC_000001.9:g.188572965A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367462.5:c.237-55462T>C MANE Select	ENSP00000356432.3:n.237-55462T>C
ENST00000367462.4:c.237-55462T>C	ENSP00000356432.3:n.237-55462T>C
ENST00000631494.1:c.237-55462T>C	ENSP00000487601.1:n.237-55462T>C
NM_199051.1:c.237-55462T>C	NP_950252.1:n.237-55462T>C
XM_005245117.1:c.237-55462T>C	XP_005245174.1:n.237-55462T>C
XM_005245118.3:c.237-55462T>C	XP_005245175.1:n.237-55462T>C
XM_005245120.2:c.237-55462T>C	XP_005245177.1:n.237-55462T>C
XM_011509472.1:c.147-55462T>C	XP_011507774.1:n.147-55462T>C
XM_011509473.1:c.147-55462T>C	XP_011507775.1:n.147-55462T>C
XM_011509474.1:c.147-55462T>C	XP_011507776.1:n.147-55462T>C
XM_011509475.1:c.108-55462T>C	XP_011507777.1:n.108-55462T>C
XM_011509476.1:c.122-72157T>C	XP_011507778.1:n.122-72157T>C
XR_922372.1:n.82-5217A>G
XR_922373.1:n.303-5217A>G
XR_922374.1:n.82-5217A>G
NM_001317188.1:c.122-72157T>C	NP_001304117.1:n.122-72157T>C
NM_199051.2:c.237-55462T>C	NP_950252.1:n.237-55462T>C
XM_011509472.2:c.147-55462T>C	XP_011507774.1:n.147-55462T>C
XM_011509475.2:c.108-55462T>C	XP_011507777.1:n.108-55462T>C
XM_011509476.2:c.122-72157T>C	XP_011507778.1:n.122-72157T>C
XM_017001125.1:c.237-55462T>C	XP_016856614.1:n.237-55462T>C
XM_017001126.1:c.237-55462T>C	XP_016856615.1:n.237-55462T>C
XM_017001127.1:c.147-55462T>C	XP_016856616.1:n.147-55462T>C
XM_017001128.1:c.147-55462T>C	XP_016856617.1:n.147-55462T>C
XM_017001129.1:c.122-72157T>C	XP_016856618.1:n.122-72157T>C
XM_017001130.1:c.122-72157T>C	XP_016856619.1:n.122-72157T>C
XM_017001131.1:c.-643-55462T>C	XP_016856620.1:n.-643-55462T>C
XM_017001132.1:c.237-55462T>C	XP_016856621.1:n.237-55462T>C
XM_017001133.1:c.237-55462T>C	XP_016856622.1:n.237-55462T>C
NM_199051.3:c.237-55462T>C MANE Select	NP_950252.1:n.237-55462T>C
NM_001317188.2:c.122-72157T>C	NP_001304117.1:n.122-72157T>C