Canonical Allele Identifier: CA375546539

Gene: CARD9

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136372044C>G , CM000671.2:g.136372044C>G	GRCh38
NC_000009.11:g.139266496C>G , CM000671.1:g.139266496C>G	GRCh37
NC_000009.10:g.138386317C>G	NCBI36
NG_021197.1:g.6638G>C , LRG_178:g.6638G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641290.2:n.114-74G>C
ENST00000695905.1:n.163G>C
ENST00000695906.1:n.163G>C
ENST00000695908.1:n.154G>C
ENST00000696169.1:c.35G>C	ENSP00000512460.1:p.Ser12Thr
ENST00000371732.10:c.35G>C MANE Select	ENSP00000360797.5:p.Ser12Thr
ENST00000641290.1:c.-204-74G>C	ENSP00000493113.1:n.-204-74G>C
ENST00000371732.9:c.35G>C	ENSP00000360797.5:p.Ser12Thr
ENST00000371734.7:c.35G>C	ENSP00000360799.3:p.Ser12Thr
ENST00000481053.5:n.164G>C
ENST00000489932.2:c.35G>C	ENSP00000451368.1:p.Ser12Thr
ENST00000556340.1:n.166G>C
NM_052813.4:c.35G>C , LRG_178t1:c.35G>C	NP_434700.2:p.Ser12Thr
NM_052814.3:c.35G>C	NP_434701.1:p.Ser12Thr
NM_052813.5:c.35G>C MANE Select	NP_434700.2:p.Ser12Thr
NM_052814.4:c.35G>C	NP_434701.1:p.Ser12Thr