Canonical Allele Identifier: CA412447503

Gene: ASB9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.15252292C>G , CM000685.2:g.15252292C>G	GRCh38
NC_000023.10:g.15270414C>G , CM000685.1:g.15270414C>G	GRCh37
NC_000023.9:g.15180335C>G	NCBI36
NG_016218.1:g.23176G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001031739.3:c.395G>C MANE Select	NP_001026909.1:p.Ser132Thr
ENST00000380488.9:c.395G>C MANE Select	ENSP00000369855.4:p.Ser132Thr
NM_001031739.2:c.395G>C	NP_001026909.1:p.Ser132Thr
NM_001168530.1:c.395G>C	NP_001162002.1:p.Ser132Thr
NM_001168530.2:c.395G>C	NP_001162002.1:p.Ser132Thr
NM_001168531.1:c.395G>C	NP_001162003.1:p.Ser132Thr
NM_001168531.2:c.395G>C	NP_001162003.1:p.Ser132Thr
NM_024087.2:c.395G>C	NP_076992.1:p.Ser132Thr
NM_024087.3:c.395G>C	NP_076992.1:p.Ser132Thr
ENST00000380483.7:c.395G>C	ENSP00000369850.3:p.Ser132Thr
ENST00000380485.7:c.395G>C	ENSP00000369852.3:p.Ser132Thr
ENST00000380488.8:c.395G>C	ENSP00000369855.4:p.Ser132Thr
ENST00000470015.1:n.571G>C
ENST00000473862.5:n.447G>C
ENST00000477346.6:c.142G>C
ENST00000481384.5:n.480G>C
ENST00000484017.5:n.330G>C
ENST00000546332.1:c.395G>C	ENSP00000438943.1:p.Ser132Thr
XM_005274446.1:c.395G>C	XP_005274503.1:p.Ser132Thr
XM_011545458.1:c.308G>C	XP_011543760.1:p.Ser103Thr
XM_011545459.1:c.395G>C	XP_011543761.1:p.Ser132Thr
XM_011545460.1:c.308G>C	XP_011543762.1:p.Ser103Thr
XM_017029283.1:c.644G>C	XP_016884772.1:p.Ser215Thr
XM_017029284.1:c.557G>C	XP_016884773.1:p.Ser186Thr
XM_017029285.1:c.644G>C	XP_016884774.1:p.Ser215Thr
XM_017029286.2:c.644G>C	XP_016884775.1:p.Ser215Thr
XM_024452341.1:c.557G>C	XP_024308109.1:p.Ser186Thr