Canonical Allele Identifier: CA370954218

Gene: RBPMS

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.30544563C>T , CM000670.2:g.30544563C>T	GRCh38
NC_000008.10:g.30402080C>T , CM000670.1:g.30402080C>T	GRCh37
NC_000008.9:g.30521622C>T	NCBI36
NG_029534.1:g.165137C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397323.9:c.467C>T MANE Select	ENSP00000380486.4:p.Ala156Val
ENST00000287771.9:c.467C>T	ENSP00000287771.5:p.Ala156Val
ENST00000320203.8:c.467C>T	ENSP00000318102.4:p.Ala156Val
ENST00000339877.8:c.467C>T	ENSP00000340176.4:p.Ala156Val
ENST00000397323.8:c.467C>T	ENSP00000380486.4:p.Ala156Val
ENST00000517860.5:c.467C>T	ENSP00000428675.1:p.Ala156Val
ENST00000519359.5:c.540C>T
ENST00000519647.5:c.155C>T	ENSP00000430342.1:p.Ala52Val
ENST00000520161.5:c.155C>T	ENSP00000427896.1:p.Ala52Val
ENST00000520191.5:c.155C>T	ENSP00000430638.1:p.Ala52Val
ENST00000522694.1:c.269C>T	ENSP00000430893.1:p.Ala90Val
ENST00000523717.5:n.827C>T
NM_001008710.2:c.467C>T	NP_001008710.1:p.Ala156Val
NM_001008711.2:c.467C>T	NP_001008711.1:p.Ala156Val
NM_001008712.2:c.467C>T	NP_001008712.1:p.Ala156Val
NM_006867.3:c.467C>T	NP_006858.1:p.Ala156Val
XM_006716277.2:c.467C>T	XP_006716340.1:p.Ala156Val
XM_011544372.1:c.467C>T	XP_011542674.1:p.Ala156Val
XM_011544373.1:c.467C>T	XP_011542675.1:p.Ala156Val
XM_011544374.1:c.467C>T	XP_011542676.1:p.Ala156Val
XM_011544375.1:c.467C>T	XP_011542677.1:p.Ala156Val
XM_011544376.1:c.467C>T	XP_011542678.1:p.Ala156Val
XM_011544377.1:c.287C>T	XP_011542679.1:p.Ala96Val
XM_011544378.1:c.467C>T	XP_011542680.1:p.Ala156Val
XM_011544379.1:c.467C>T	XP_011542681.1:p.Ala156Val
XM_011544380.1:c.467C>T	XP_011542682.1:p.Ala156Val
XM_011544381.1:c.398-14324C>T	XP_011542683.1:n.398-14324C>T
XM_011544382.1:c.398-2729C>T	XP_011542684.1:n.398-2729C>T
XM_017012980.2:c.467C>T	XP_016868469.1:p.Ala156Val
XM_017012981.2:c.467C>T	XP_016868470.1:p.Ala156Val
XM_017012982.2:c.467C>T	XP_016868471.1:p.Ala156Val
XM_017012983.2:c.410C>T	XP_016868472.1:p.Ala137Val
XM_017012984.2:c.467C>T	XP_016868473.1:p.Ala156Val
XM_017012985.2:c.281C>T	XP_016868474.1:p.Ala94Val
XM_017012986.2:c.467C>T	XP_016868475.1:p.Ala156Val
XM_017012987.2:c.398-14324C>T	XP_016868476.1:n.398-14324C>T
XM_017012988.2:c.467C>T	XP_016868477.1:p.Ala156Val
XM_017012989.2:c.467C>T	XP_016868478.1:p.Ala156Val
XM_017012990.2:c.398-14324C>T	XP_016868479.1:n.398-14324C>T
XM_017012991.2:c.155C>T	XP_016868480.1:p.Ala52Val
XM_017012992.2:c.398-2729C>T	XP_016868481.1:n.398-2729C>T
XM_024447054.1:c.287C>T	XP_024302822.1:p.Ala96Val
XM_024447055.1:c.281C>T	XP_024302823.1:p.Ala94Val
XR_001745460.2:n.1019C>T
XR_001745461.2:n.1019C>T
XR_001745462.2:n.950-14324C>T
XR_001745463.2:n.950-14324C>T
NM_001008710.3:c.467C>T MANE Select	NP_001008710.1:p.Ala156Val
NM_001008711.3:c.467C>T	NP_001008711.1:p.Ala156Val
NM_006867.4:c.467C>T	NP_006858.1:p.Ala156Val
NM_001008712.3:c.467C>T	NP_001008712.1:p.Ala156Val