Canonical Allele Identifier: CA357401924

Gene: BMP2K PAQR3

Linked Data

• dbSNP Id: rs1346083538
• gnomAD v2: 4-79832469-C-T
• MyVariant Identifiers: chr4:g.79832469C>T (hg19) ; chr4:g.78911315C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78911315C>T , CM000666.2:g.78911315C>T	GRCh38
NC_000004.11:g.79832469C>T , CM000666.1:g.79832469C>T	GRCh37
NC_000004.10:g.80051493C>T	NCBI36
NG_047162.1:g.139938C>T
NG_053104.1:g.33124G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502613.3:c.2768C>T (BMP2K) MANE Select	ENSP00000424668.2:p.Pro923Leu
ENST00000335016.9:c.2768C>T (BMP2K)	ENSP00000334836.5:p.Pro923Leu
ENST00000342820.10:c.*782+3895G>A (PAQR3)	ENSP00000344203.6:n.*782+3895G>A
ENST00000502613.1:c.1845C>T (BMP2K)
ENST00000511594.5:c.*874G>A (PAQR3)	ENSP00000425080.1:n.*874G>A
ENST00000512760.5:c.*792+3895G>A (PAQR3)	ENSP00000426875.1:n.*792+3895G>A
ENST00000628286.1:c.*1744C>T (BMP2K)	ENSP00000487317.1:n.*1744C>T
NM_198892.1:c.2768C>T (BMP2K)	NP_942595.1:p.Pro923Leu
XM_005263117.1:c.2657C>T (BMP2K)	XP_005263174.1:p.Pro886Leu
XM_011532101.1:c.2528C>T (BMP2K)	XP_011530403.1:p.Pro843Leu
XR_938694.1:n.1118-5154G>A (PAQR3)
XM_017008381.1:c.2528C>T (BMP2K)	XP_016863870.1:p.Pro843Leu
XM_017008382.1:c.1880C>T (BMP2K)	XP_016863871.1:p.Pro627Leu
XR_938694.3:n.1098-5154G>A (PAQR3)
NM_198892.2:c.2768C>T (BMP2K) MANE Select	NP_942595.1:p.Pro923Leu