Canonical Allele Identifier: CA357402731

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78911420C>A , CM000666.2:g.78911420C>A GRCh38
NC_000004.11:g.79832574C>A , CM000666.1:g.79832574C>A GRCh37
NC_000004.10:g.80051598C>A NCBI36
NG_047162.1:g.140043C>A
NG_053104.1:g.33019G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000502613.3:c.2873C>A (BMP2K) MANE Select ENSP00000424668.2:p.Pro958His
ENST00000335016.9:c.2873C>A (BMP2K) ENSP00000334836.5:p.Pro958His
ENST00000342820.10:c.*782+3790G>T (PAQR3) ENSP00000344203.6:n.*782+3790G>T
ENST00000502613.1:c.1950C>A (BMP2K)
ENST00000511594.5:c.*769G>T (PAQR3) ENSP00000425080.1:n.*769G>T
ENST00000512760.5:c.*792+3790G>T (PAQR3) ENSP00000426875.1:n.*792+3790G>T
ENST00000628286.1:c.*1849C>A (BMP2K) ENSP00000487317.1:n.*1849C>A
NM_198892.1:c.2873C>A (BMP2K) NP_942595.1:p.Pro958His
XM_005263117.1:c.2762C>A (BMP2K) XP_005263174.1:p.Pro921His
XM_011532101.1:c.2633C>A (BMP2K) XP_011530403.1:p.Pro878His
XR_938694.1:n.1118-5259G>T (PAQR3)
XM_017008381.1:c.2633C>A (BMP2K) XP_016863870.1:p.Pro878His
XM_017008382.1:c.1985C>A (BMP2K) XP_016863871.1:p.Pro662His
XR_938694.3:n.1098-5259G>T (PAQR3)
NM_198892.2:c.2873C>A (BMP2K) MANE Select NP_942595.1:p.Pro958His