Canonical Allele Identifier: CA357402245

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78911361G>C , CM000666.2:g.78911361G>C GRCh38
NC_000004.11:g.79832515G>C , CM000666.1:g.79832515G>C GRCh37
NC_000004.10:g.80051539G>C NCBI36
NG_047162.1:g.139984G>C
NG_053104.1:g.33078C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000502613.3:c.2814G>C (BMP2K) MANE Select ENSP00000424668.2:p.Gln938His
ENST00000335016.9:c.2814G>C (BMP2K) ENSP00000334836.5:p.Gln938His
ENST00000342820.10:c.*782+3849C>G (PAQR3) ENSP00000344203.6:n.*782+3849C>G
ENST00000502613.1:c.1891G>C (BMP2K)
ENST00000511594.5:c.*828C>G (PAQR3) ENSP00000425080.1:n.*828C>G
ENST00000512760.5:c.*792+3849C>G (PAQR3) ENSP00000426875.1:n.*792+3849C>G
ENST00000628286.1:c.*1790G>C (BMP2K) ENSP00000487317.1:n.*1790G>C
NM_198892.1:c.2814G>C (BMP2K) NP_942595.1:p.Gln938His
XM_005263117.1:c.2703G>C (BMP2K) XP_005263174.1:p.Gln901His
XM_011532101.1:c.2574G>C (BMP2K) XP_011530403.1:p.Gln858His
XR_938694.1:n.1118-5200C>G (PAQR3)
XM_017008381.1:c.2574G>C (BMP2K) XP_016863870.1:p.Gln858His
XM_017008382.1:c.1926G>C (BMP2K) XP_016863871.1:p.Gln642His
XR_938694.3:n.1098-5200C>G (PAQR3)
NM_198892.2:c.2814G>C (BMP2K) MANE Select NP_942595.1:p.Gln938His