Canonical Allele Identifier: CA399516743

Gene: FKBP10

Linked Data

• MyVariant Identifiers: chr17:g.39975821G>C (hg19) ; chr17:g.41819569G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41819569G>C , CM000679.2:g.41819569G>C	GRCh38
NC_000017.10:g.39975821G>C , CM000679.1:g.39975821G>C	GRCh37
NC_000017.9:g.37229347G>C	NCBI36
NG_015860.1:g.11860G>C , LRG_12:g.11860G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706683.1:c.728-700G>C	ENSP00000516497.1:n.728-700G>C
ENST00000321562.9:c.957G>C MANE Select	ENSP00000317232.4:p.Gln319His
ENST00000321562.8:c.957G>C	ENSP00000317232.4:p.Gln319His
ENST00000455106.1:c.185G>C
ENST00000487489.1:n.570G>C
ENST00000489591.5:c.*367G>C	ENSP00000466352.1:n.*367G>C
NM_021939.3:c.957G>C , LRG_12t1:c.957G>C	NP_068758.3:p.Gln319His
XM_011525099.1:c.957G>C	XP_011523401.1:p.Gln319His
XM_011525100.1:c.684G>C	XP_011523402.1:p.Gln228His
XM_011525099.3:c.957G>C	XP_011523401.1:p.Gln319His
XM_011525100.2:c.684G>C	XP_011523402.1:p.Gln228His
NM_021939.4:c.957G>C MANE Select	NP_068758.3:p.Gln319His