Canonical Allele Identifier: CA357404632

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78911719G>A , CM000666.2:g.78911719G>A GRCh38
NC_000004.11:g.79832873G>A , CM000666.1:g.79832873G>A GRCh37
NC_000004.10:g.80051897G>A NCBI36
NG_047162.1:g.140342G>A
NG_053104.1:g.32720C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000502613.3:c.3172G>A (BMP2K) MANE Select ENSP00000424668.2:p.Val1058Ile
ENST00000335016.9:c.3172G>A (BMP2K) ENSP00000334836.5:p.Val1058Ile
ENST00000342820.10:c.*782+3491C>T (PAQR3) ENSP00000344203.6:n.*782+3491C>T
ENST00000502613.1:c.2249G>A (BMP2K)
ENST00000511594.5:c.*470C>T (PAQR3) ENSP00000425080.1:n.*470C>T
ENST00000512760.5:c.*792+3491C>T (PAQR3) ENSP00000426875.1:n.*792+3491C>T
ENST00000628286.1:c.*2148G>A (BMP2K) ENSP00000487317.1:n.*2148G>A
NM_198892.1:c.3172G>A (BMP2K) NP_942595.1:p.Val1058Ile
XM_005263117.1:c.3061G>A (BMP2K) XP_005263174.1:p.Val1021Ile
XM_011532101.1:c.2932G>A (BMP2K) XP_011530403.1:p.Val978Ile
XR_938694.1:n.1118-5558C>T (PAQR3)
XM_017008381.1:c.2932G>A (BMP2K) XP_016863870.1:p.Val978Ile
XM_017008382.1:c.2284G>A (BMP2K) XP_016863871.1:p.Val762Ile
XR_938694.3:n.1098-5558C>T (PAQR3)
NM_198892.2:c.3172G>A (BMP2K) MANE Select NP_942595.1:p.Val1058Ile