Canonical Allele Identifier: CA357402930

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78911448G>C , CM000666.2:g.78911448G>C GRCh38
NC_000004.11:g.79832602G>C , CM000666.1:g.79832602G>C GRCh37
NC_000004.10:g.80051626G>C NCBI36
NG_047162.1:g.140071G>C
NG_053104.1:g.32991C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000502613.3:c.2901G>C (BMP2K) MANE Select ENSP00000424668.2:p.Gln967His
ENST00000335016.9:c.2901G>C (BMP2K) ENSP00000334836.5:p.Gln967His
ENST00000342820.10:c.*782+3762C>G (PAQR3) ENSP00000344203.6:n.*782+3762C>G
ENST00000502613.1:c.1978G>C (BMP2K)
ENST00000511594.5:c.*741C>G (PAQR3) ENSP00000425080.1:n.*741C>G
ENST00000512760.5:c.*792+3762C>G (PAQR3) ENSP00000426875.1:n.*792+3762C>G
ENST00000628286.1:c.*1877G>C (BMP2K) ENSP00000487317.1:n.*1877G>C
NM_198892.1:c.2901G>C (BMP2K) NP_942595.1:p.Gln967His
XM_005263117.1:c.2790G>C (BMP2K) XP_005263174.1:p.Gln930His
XM_011532101.1:c.2661G>C (BMP2K) XP_011530403.1:p.Gln887His
XR_938694.1:n.1118-5287C>G (PAQR3)
XM_017008381.1:c.2661G>C (BMP2K) XP_016863870.1:p.Gln887His
XM_017008382.1:c.2013G>C (BMP2K) XP_016863871.1:p.Gln671His
XR_938694.3:n.1098-5287C>G (PAQR3)
NM_198892.2:c.2901G>C (BMP2K) MANE Select NP_942595.1:p.Gln967His