Canonical Allele Identifier: CA357403237

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78911494A>G , CM000666.2:g.78911494A>G GRCh38
NC_000004.11:g.79832648A>G , CM000666.1:g.79832648A>G GRCh37
NC_000004.10:g.80051672A>G NCBI36
NG_047162.1:g.140117A>G
NG_053104.1:g.32945T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000502613.3:c.2947A>G (BMP2K) MANE Select ENSP00000424668.2:p.Arg983Gly
ENST00000335016.9:c.2947A>G (BMP2K) ENSP00000334836.5:p.Arg983Gly
ENST00000342820.10:c.*782+3716T>C (PAQR3) ENSP00000344203.6:n.*782+3716T>C
ENST00000502613.1:c.2024A>G (BMP2K)
ENST00000511594.5:c.*695T>C (PAQR3) ENSP00000425080.1:n.*695T>C
ENST00000512760.5:c.*792+3716T>C (PAQR3) ENSP00000426875.1:n.*792+3716T>C
ENST00000628286.1:c.*1923A>G (BMP2K) ENSP00000487317.1:n.*1923A>G
NM_198892.1:c.2947A>G (BMP2K) NP_942595.1:p.Arg983Gly
XM_005263117.1:c.2836A>G (BMP2K) XP_005263174.1:p.Arg946Gly
XM_011532101.1:c.2707A>G (BMP2K) XP_011530403.1:p.Arg903Gly
XR_938694.1:n.1118-5333T>C (PAQR3)
XM_017008381.1:c.2707A>G (BMP2K) XP_016863870.1:p.Arg903Gly
XM_017008382.1:c.2059A>G (BMP2K) XP_016863871.1:p.Arg687Gly
XR_938694.3:n.1098-5333T>C (PAQR3)
NM_198892.2:c.2947A>G (BMP2K) MANE Select NP_942595.1:p.Arg983Gly