Canonical Allele Identifier: CA357403265

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78911498G>T , CM000666.2:g.78911498G>T GRCh38
NC_000004.11:g.79832652G>T , CM000666.1:g.79832652G>T GRCh37
NC_000004.10:g.80051676G>T NCBI36
NG_047162.1:g.140121G>T
NG_053104.1:g.32941C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000502613.3:c.2951G>T (BMP2K) MANE Select ENSP00000424668.2:p.Arg984Leu
ENST00000335016.9:c.2951G>T (BMP2K) ENSP00000334836.5:p.Arg984Leu
ENST00000342820.10:c.*782+3712C>A (PAQR3) ENSP00000344203.6:n.*782+3712C>A
ENST00000502613.1:c.2028G>T (BMP2K)
ENST00000511594.5:c.*691C>A (PAQR3) ENSP00000425080.1:n.*691C>A
ENST00000512760.5:c.*792+3712C>A (PAQR3) ENSP00000426875.1:n.*792+3712C>A
ENST00000628286.1:c.*1927G>T (BMP2K) ENSP00000487317.1:n.*1927G>T
NM_198892.1:c.2951G>T (BMP2K) NP_942595.1:p.Arg984Leu
XM_005263117.1:c.2840G>T (BMP2K) XP_005263174.1:p.Arg947Leu
XM_011532101.1:c.2711G>T (BMP2K) XP_011530403.1:p.Arg904Leu
XR_938694.1:n.1118-5337C>A (PAQR3)
XM_017008381.1:c.2711G>T (BMP2K) XP_016863870.1:p.Arg904Leu
XM_017008382.1:c.2063G>T (BMP2K) XP_016863871.1:p.Arg688Leu
XR_938694.3:n.1098-5337C>A (PAQR3)
NM_198892.2:c.2951G>T (BMP2K) MANE Select NP_942595.1:p.Arg984Leu