Canonical Allele Identifier: CA440225907

Linked Data

MyVariant Identifiers: chr4:g.79832587A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78911433A>C , CM000666.2:g.78911433A>C GRCh38
NC_000004.11:g.79832587A>C , CM000666.1:g.79832587A>C GRCh37
NC_000004.10:g.80051611A>C NCBI36
NG_047162.1:g.140056A>C
NG_053104.1:g.33006T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000502613.3:c.2886A>C (BMP2K) MANE Select ENSP00000424668.2:p.Ile962=
ENST00000335016.9:c.2886A>C (BMP2K) ENSP00000334836.5:p.Ile962=
ENST00000342820.10:c.*782+3777T>G (PAQR3) ENSP00000344203.6:n.*782+3777T>G
ENST00000502613.1:c.1963A>C (BMP2K)
ENST00000511594.5:c.*756T>G (PAQR3) ENSP00000425080.1:n.*756T>G
ENST00000512760.5:c.*792+3777T>G (PAQR3) ENSP00000426875.1:n.*792+3777T>G
ENST00000628286.1:c.*1862A>C (BMP2K) ENSP00000487317.1:n.*1862A>C
NM_198892.1:c.2886A>C (BMP2K) NP_942595.1:p.Ile962=
XM_005263117.1:c.2775A>C (BMP2K) XP_005263174.1:p.Ile925=
XM_011532101.1:c.2646A>C (BMP2K) XP_011530403.1:p.Ile882=
XR_938694.1:n.1118-5272T>G (PAQR3)
XM_017008381.1:c.2646A>C (BMP2K) XP_016863870.1:p.Ile882=
XM_017008382.1:c.1998A>C (BMP2K) XP_016863871.1:p.Ile666=
XR_938694.3:n.1098-5272T>G (PAQR3)
NM_198892.2:c.2886A>C (BMP2K) MANE Select NP_942595.1:p.Ile962=