Canonical Allele Identifier: CA440225868

Linked Data

MyVariant Identifiers: chr4:g.79832533A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78911379A>T , CM000666.2:g.78911379A>T GRCh38
NC_000004.11:g.79832533A>T , CM000666.1:g.79832533A>T GRCh37
NC_000004.10:g.80051557A>T NCBI36
NG_047162.1:g.140002A>T
NG_053104.1:g.33060T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000502613.3:c.2832A>T (BMP2K) MANE Select ENSP00000424668.2:p.Thr944=
ENST00000335016.9:c.2832A>T (BMP2K) ENSP00000334836.5:p.Thr944=
ENST00000342820.10:c.*782+3831T>A (PAQR3) ENSP00000344203.6:n.*782+3831T>A
ENST00000502613.1:c.1909A>T (BMP2K)
ENST00000511594.5:c.*810T>A (PAQR3) ENSP00000425080.1:n.*810T>A
ENST00000512760.5:c.*792+3831T>A (PAQR3) ENSP00000426875.1:n.*792+3831T>A
ENST00000628286.1:c.*1808A>T (BMP2K) ENSP00000487317.1:n.*1808A>T
NM_198892.1:c.2832A>T (BMP2K) NP_942595.1:p.Thr944=
XM_005263117.1:c.2721A>T (BMP2K) XP_005263174.1:p.Thr907=
XM_011532101.1:c.2592A>T (BMP2K) XP_011530403.1:p.Thr864=
XR_938694.1:n.1118-5218T>A (PAQR3)
XM_017008381.1:c.2592A>T (BMP2K) XP_016863870.1:p.Thr864=
XM_017008382.1:c.1944A>T (BMP2K) XP_016863871.1:p.Thr648=
XR_938694.3:n.1098-5218T>A (PAQR3)
NM_198892.2:c.2832A>T (BMP2K) MANE Select NP_942595.1:p.Thr944=