Canonical Allele Identifier: CA357403993

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78911590C>G , CM000666.2:g.78911590C>G GRCh38
NC_000004.11:g.79832744C>G , CM000666.1:g.79832744C>G GRCh37
NC_000004.10:g.80051768C>G NCBI36
NG_047162.1:g.140213C>G
NG_053104.1:g.32849G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000502613.3:c.3043C>G (BMP2K) MANE Select ENSP00000424668.2:p.Pro1015Ala
ENST00000335016.9:c.3043C>G (BMP2K) ENSP00000334836.5:p.Pro1015Ala
ENST00000342820.10:c.*782+3620G>C (PAQR3) ENSP00000344203.6:n.*782+3620G>C
ENST00000502613.1:c.2120C>G (BMP2K)
ENST00000511594.5:c.*599G>C (PAQR3) ENSP00000425080.1:n.*599G>C
ENST00000512760.5:c.*792+3620G>C (PAQR3) ENSP00000426875.1:n.*792+3620G>C
ENST00000628286.1:c.*2019C>G (BMP2K) ENSP00000487317.1:n.*2019C>G
NM_198892.1:c.3043C>G (BMP2K) NP_942595.1:p.Pro1015Ala
XM_005263117.1:c.2932C>G (BMP2K) XP_005263174.1:p.Pro978Ala
XM_011532101.1:c.2803C>G (BMP2K) XP_011530403.1:p.Pro935Ala
XR_938694.1:n.1118-5429G>C (PAQR3)
XM_017008381.1:c.2803C>G (BMP2K) XP_016863870.1:p.Pro935Ala
XM_017008382.1:c.2155C>G (BMP2K) XP_016863871.1:p.Pro719Ala
XR_938694.3:n.1098-5429G>C (PAQR3)
NM_198892.2:c.3043C>G (BMP2K) MANE Select NP_942595.1:p.Pro1015Ala