Canonical Allele Identifier: CA357403478

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78911528G>C , CM000666.2:g.78911528G>C GRCh38
NC_000004.11:g.79832682G>C , CM000666.1:g.79832682G>C GRCh37
NC_000004.10:g.80051706G>C NCBI36
NG_047162.1:g.140151G>C
NG_053104.1:g.32911C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000502613.3:c.2981G>C (BMP2K) MANE Select ENSP00000424668.2:p.Gly994Ala
ENST00000335016.9:c.2981G>C (BMP2K) ENSP00000334836.5:p.Gly994Ala
ENST00000342820.10:c.*782+3682C>G (PAQR3) ENSP00000344203.6:n.*782+3682C>G
ENST00000502613.1:c.2058G>C (BMP2K)
ENST00000511594.5:c.*661C>G (PAQR3) ENSP00000425080.1:n.*661C>G
ENST00000512760.5:c.*792+3682C>G (PAQR3) ENSP00000426875.1:n.*792+3682C>G
ENST00000628286.1:c.*1957G>C (BMP2K) ENSP00000487317.1:n.*1957G>C
NM_198892.1:c.2981G>C (BMP2K) NP_942595.1:p.Gly994Ala
XM_005263117.1:c.2870G>C (BMP2K) XP_005263174.1:p.Gly957Ala
XM_011532101.1:c.2741G>C (BMP2K) XP_011530403.1:p.Gly914Ala
XR_938694.1:n.1118-5367C>G (PAQR3)
XM_017008381.1:c.2741G>C (BMP2K) XP_016863870.1:p.Gly914Ala
XM_017008382.1:c.2093G>C (BMP2K) XP_016863871.1:p.Gly698Ala
XR_938694.3:n.1098-5367C>G (PAQR3)
NM_198892.2:c.2981G>C (BMP2K) MANE Select NP_942595.1:p.Gly994Ala