Canonical Allele Identifier: CA440226356

Linked Data

MyVariant Identifiers: chr4:g.79832470T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78911316T>G , CM000666.2:g.78911316T>G GRCh38
NC_000004.11:g.79832470T>G , CM000666.1:g.79832470T>G GRCh37
NC_000004.10:g.80051494T>G NCBI36
NG_047162.1:g.139939T>G
NG_053104.1:g.33123A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000502613.3:c.2769T>G (BMP2K) MANE Select ENSP00000424668.2:p.Pro923=
ENST00000335016.9:c.2769T>G (BMP2K) ENSP00000334836.5:p.Pro923=
ENST00000342820.10:c.*782+3894A>C (PAQR3) ENSP00000344203.6:n.*782+3894A>C
ENST00000502613.1:c.1846T>G (BMP2K)
ENST00000511594.5:c.*873A>C (PAQR3) ENSP00000425080.1:n.*873A>C
ENST00000512760.5:c.*792+3894A>C (PAQR3) ENSP00000426875.1:n.*792+3894A>C
ENST00000628286.1:c.*1745T>G (BMP2K) ENSP00000487317.1:n.*1745T>G
NM_198892.1:c.2769T>G (BMP2K) NP_942595.1:p.Pro923=
XM_005263117.1:c.2658T>G (BMP2K) XP_005263174.1:p.Pro886=
XM_011532101.1:c.2529T>G (BMP2K) XP_011530403.1:p.Pro843=
XR_938694.1:n.1118-5155A>C (PAQR3)
XM_017008381.1:c.2529T>G (BMP2K) XP_016863870.1:p.Pro843=
XM_017008382.1:c.1881T>G (BMP2K) XP_016863871.1:p.Pro627=
XR_938694.3:n.1098-5155A>C (PAQR3)
NM_198892.2:c.2769T>G (BMP2K) MANE Select NP_942595.1:p.Pro923=