Canonical Allele Identifier: CA2678874300

Linked Data

gnomAD v4: 6-43523224-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43523224T>C , CM000668.2:g.43523224T>C GRCh38
NC_000006.11:g.43490962T>C , CM000668.1:g.43490962T>C GRCh37
NC_000006.10:g.43598940T>C NCBI36
NG_028283.1:g.11186T>C
NG_028283.3:g.18523T>C
NG_051658.1:g.57852A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000265351.12:c.*644A>G (XPO5) MANE Select ENSP00000265351.7:n.*644A>G
ENST00000607635.2:c.922+2176T>C (POLR1C) ENSP00000496683.1:n.922+2176T>C
ENST00000643341.1:c.922+2176T>C (POLR1C) ENSP00000496018.1:n.922+2176T>C
ENST00000643799.1:c.*17+1907T>C (POLR1C) ENSP00000494529.1:n.*17+1907T>C
ENST00000646433.1:c.922+2176T>C (POLR1C) ENSP00000494368.1:n.922+2176T>C
ENST00000646700.1:c.922+2176T>C (POLR1C) ENSP00000495521.1:n.922+2176T>C
ENST00000265351.11:c.*644A>G (XPO5) ENSP00000265351.7:n.*644A>G
ENST00000304004.7:c.922+2176T>C (POLR1C) ENSP00000307212.3:n.922+2176T>C
ENST00000455854.2:n.2742A>G (XPO5)
NM_020750.2:c.*644A>G (XPO5) NP_065801.1:n.*644A>G
XM_005249491.1:c.922+2176T>C (POLR1C) XP_005249548.1:n.922+2176T>C
XM_011515000.1:c.922+2176T>C (POLR1C) XP_011513302.1:n.922+2176T>C
NM_001318876.1:c.922+2176T>C (POLR1C) NP_001305805.1:n.922+2176T>C
NM_001363658.1:c.922+2176T>C (POLR1C) NP_001350587.1:n.922+2176T>C
NR_144392.1:n.4608A>G (XPO5)
NM_020750.3:c.*644A>G (XPO5) MANE Select NP_065801.1:n.*644A>G
NM_001363658.2:c.922+2176T>C (POLR1C) NP_001350587.1:n.922+2176T>C
NM_001318876.2:c.922+2176T>C (POLR1C) NP_001305805.1:n.922+2176T>C
NR_144392.2:n.4571A>G (XPO5)