Canonical Allele Identifier: CA357401796

Linked Data

dbSNP Id: rs1734581830

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78911297C>T , CM000666.2:g.78911297C>T GRCh38
NC_000004.11:g.79832451C>T , CM000666.1:g.79832451C>T GRCh37
NC_000004.10:g.80051475C>T NCBI36
NG_047162.1:g.139920C>T
NG_053104.1:g.33142G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000502613.3:c.2750C>T (BMP2K) MANE Select ENSP00000424668.2:p.Pro917Leu
ENST00000335016.9:c.2750C>T (BMP2K) ENSP00000334836.5:p.Pro917Leu
ENST00000342820.10:c.*782+3913G>A (PAQR3) ENSP00000344203.6:n.*782+3913G>A
ENST00000502613.1:c.1827C>T (BMP2K)
ENST00000511594.5:c.*892G>A (PAQR3) ENSP00000425080.1:n.*892G>A
ENST00000512760.5:c.*792+3913G>A (PAQR3) ENSP00000426875.1:n.*792+3913G>A
ENST00000628286.1:c.*1726C>T (BMP2K) ENSP00000487317.1:n.*1726C>T
NM_198892.1:c.2750C>T (BMP2K) NP_942595.1:p.Pro917Leu
XM_005263117.1:c.2639C>T (BMP2K) XP_005263174.1:p.Pro880Leu
XM_011532101.1:c.2510C>T (BMP2K) XP_011530403.1:p.Pro837Leu
XR_938694.1:n.1118-5136G>A (PAQR3)
XM_017008381.1:c.2510C>T (BMP2K) XP_016863870.1:p.Pro837Leu
XM_017008382.1:c.1862C>T (BMP2K) XP_016863871.1:p.Pro621Leu
XR_938694.3:n.1098-5136G>A (PAQR3)
NM_198892.2:c.2750C>T (BMP2K) MANE Select NP_942595.1:p.Pro917Leu