Canonical Allele Identifier: CA357401686

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78911285A>C , CM000666.2:g.78911285A>C GRCh38
NC_000004.11:g.79832439A>C , CM000666.1:g.79832439A>C GRCh37
NC_000004.10:g.80051463A>C NCBI36
NG_047162.1:g.139908A>C
NG_053104.1:g.33154T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000502613.3:c.2738A>C (BMP2K) MANE Select ENSP00000424668.2:p.His913Pro
ENST00000335016.9:c.2738A>C (BMP2K) ENSP00000334836.5:p.His913Pro
ENST00000342820.10:c.*782+3925T>G (PAQR3) ENSP00000344203.6:n.*782+3925T>G
ENST00000502613.1:c.1815A>C (BMP2K)
ENST00000511594.5:c.*904T>G (PAQR3) ENSP00000425080.1:n.*904T>G
ENST00000512760.5:c.*792+3925T>G (PAQR3) ENSP00000426875.1:n.*792+3925T>G
ENST00000628286.1:c.*1714A>C (BMP2K) ENSP00000487317.1:n.*1714A>C
NM_198892.1:c.2738A>C (BMP2K) NP_942595.1:p.His913Pro
XM_005263117.1:c.2627A>C (BMP2K) XP_005263174.1:p.His876Pro
XM_011532101.1:c.2498A>C (BMP2K) XP_011530403.1:p.His833Pro
XR_938694.1:n.1118-5124T>G (PAQR3)
XM_017008381.1:c.2498A>C (BMP2K) XP_016863870.1:p.His833Pro
XM_017008382.1:c.1850A>C (BMP2K) XP_016863871.1:p.His617Pro
XR_938694.3:n.1098-5124T>G (PAQR3)
NM_198892.2:c.2738A>C (BMP2K) MANE Select NP_942595.1:p.His913Pro