Canonical Allele Identifier: CA357402185

Linked Data

gnomAD v4: 4-78911351-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78911351C>T , CM000666.2:g.78911351C>T GRCh38
NC_000004.11:g.79832505C>T , CM000666.1:g.79832505C>T GRCh37
NC_000004.10:g.80051529C>T NCBI36
NG_047162.1:g.139974C>T
NG_053104.1:g.33088G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000502613.3:c.2804C>T (BMP2K) MANE Select ENSP00000424668.2:p.Thr935Ile
ENST00000335016.9:c.2804C>T (BMP2K) ENSP00000334836.5:p.Thr935Ile
ENST00000342820.10:c.*782+3859G>A (PAQR3) ENSP00000344203.6:n.*782+3859G>A
ENST00000502613.1:c.1881C>T (BMP2K)
ENST00000511594.5:c.*838G>A (PAQR3) ENSP00000425080.1:n.*838G>A
ENST00000512760.5:c.*792+3859G>A (PAQR3) ENSP00000426875.1:n.*792+3859G>A
ENST00000628286.1:c.*1780C>T (BMP2K) ENSP00000487317.1:n.*1780C>T
NM_198892.1:c.2804C>T (BMP2K) NP_942595.1:p.Thr935Ile
XM_005263117.1:c.2693C>T (BMP2K) XP_005263174.1:p.Thr898Ile
XM_011532101.1:c.2564C>T (BMP2K) XP_011530403.1:p.Thr855Ile
XR_938694.1:n.1118-5190G>A (PAQR3)
XM_017008381.1:c.2564C>T (BMP2K) XP_016863870.1:p.Thr855Ile
XM_017008382.1:c.1916C>T (BMP2K) XP_016863871.1:p.Thr639Ile
XR_938694.3:n.1098-5190G>A (PAQR3)
NM_198892.2:c.2804C>T (BMP2K) MANE Select NP_942595.1:p.Thr935Ile