Canonical Allele Identifier: CA1942339079

Gene: OAT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.124405488G= , CM000672.2:g.124405488G=	GRCh38
NC_000010.10:g.126094057G= , CM000672.1:g.126094057G=	GRCh37
NC_000010.9:g.126084047G=	NCBI36
NG_008861.1:g.18463C= , LRG_685:g.18463C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368845.6:c.596C= MANE Select	ENSP00000357838.5:p.Pro199=
ENST00000368845.5:c.596C=	ENSP00000357838.5:p.Pro199=
ENST00000467675.5:n.397C=
ENST00000483711.1:n.442C=
ENST00000539214.5:c.182C=	ENSP00000439042.1:p.Pro61=
NM_000274.3:c.596C= , LRG_685t1:c.596C=	NP_000265.1:p.Pro199=
NM_001171814.1:c.182C=	NP_001165285.1:p.Pro61=
XM_006717871.2:c.596C=	XP_006717934.1:p.Pro199=
XM_011539833.1:c.596C=	XP_011538135.1:p.Pro199=
XM_011539834.1:c.596C=	XP_011538136.1:p.Pro199=
NM_001322965.1:c.596C=	NP_001309894.1:p.Pro199=
NM_001322966.1:c.596C=	NP_001309895.1:p.Pro199=
NM_001322967.1:c.596C=	NP_001309896.1:p.Pro199=
NM_001322968.1:c.596C=	NP_001309897.1:p.Pro199=
NM_001322969.1:c.596C=	NP_001309898.1:p.Pro199=
NM_001322970.1:c.596C=	NP_001309899.1:p.Pro199=
NM_001322971.1:c.275C=	NP_001309900.1:p.Pro92=
NM_001322974.1:c.-5C=	NP_001309903.1:n.-5C=
XM_017016279.1:c.-5C=	XP_016871768.1:n.-5C=
NM_000274.4:c.596C= MANE Select	NP_000265.1:p.Pro199=
NM_001322965.2:c.596C=	NP_001309894.1:p.Pro199=
NM_001322966.2:c.596C=	NP_001309895.1:p.Pro199=
NM_001322967.2:c.596C=	NP_001309896.1:p.Pro199=
NM_001322968.2:c.596C=	NP_001309897.1:p.Pro199=
NM_001322969.2:c.596C=	NP_001309898.1:p.Pro199=
NM_001322970.2:c.596C=	NP_001309899.1:p.Pro199=
NM_001322971.2:c.275C=	NP_001309900.1:p.Pro92=
NM_001322974.2:c.-5C=	NP_001309903.1:n.-5C=
NM_001171814.2:c.182C=	NP_001165285.1:p.Pro61=