Canonical Allele Identifier: CA440225843

Linked Data

MyVariant Identifiers: chr4:g.79832506T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78911352T>A , CM000666.2:g.78911352T>A GRCh38
NC_000004.11:g.79832506T>A , CM000666.1:g.79832506T>A GRCh37
NC_000004.10:g.80051530T>A NCBI36
NG_047162.1:g.139975T>A
NG_053104.1:g.33087A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000502613.3:c.2805T>A (BMP2K) MANE Select ENSP00000424668.2:p.Thr935=
ENST00000335016.9:c.2805T>A (BMP2K) ENSP00000334836.5:p.Thr935=
ENST00000342820.10:c.*782+3858A>T (PAQR3) ENSP00000344203.6:n.*782+3858A>T
ENST00000502613.1:c.1882T>A (BMP2K)
ENST00000511594.5:c.*837A>T (PAQR3) ENSP00000425080.1:n.*837A>T
ENST00000512760.5:c.*792+3858A>T (PAQR3) ENSP00000426875.1:n.*792+3858A>T
ENST00000628286.1:c.*1781T>A (BMP2K) ENSP00000487317.1:n.*1781T>A
NM_198892.1:c.2805T>A (BMP2K) NP_942595.1:p.Thr935=
XM_005263117.1:c.2694T>A (BMP2K) XP_005263174.1:p.Thr898=
XM_011532101.1:c.2565T>A (BMP2K) XP_011530403.1:p.Thr855=
XR_938694.1:n.1118-5191A>T (PAQR3)
XM_017008381.1:c.2565T>A (BMP2K) XP_016863870.1:p.Thr855=
XM_017008382.1:c.1917T>A (BMP2K) XP_016863871.1:p.Thr639=
XR_938694.3:n.1098-5191A>T (PAQR3)
NM_198892.2:c.2805T>A (BMP2K) MANE Select NP_942595.1:p.Thr935=