Canonical Allele Identifier: CA1397839655

Gene: CASR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122188481A= , CM000665.2:g.122188481A=	GRCh38
NC_000003.11:g.121907328A= , CM000665.1:g.121907328A=	GRCh37
NC_000003.10:g.123390018A=	NCBI36
NG_009058.1:g.9799A=
NG_009058.2:g.9814A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000498619.4:c.-243+3952A=	ENSP00000420194.1:n.-243+3952A=
ENST00000638421.1:c.-243+3952A=	ENSP00000492190.1:n.-243+3952A=
ENST00000639785.2:c.-243+4669A= MANE Select	ENSP00000491584.2:n.-243+4669A=
ENST00000643573.1:n.98+3952A=
ENST00000490131.5:c.-243+4669A=	ENSP00000418685.1:n.-243+4669A=
ENST00000498619.2:c.-243+3952A=	ENSP00000420194.1:n.-243+3952A=
NM_000388.3:c.-243+4669A=	NP_000379.2:n.-243+4669A=
NM_001178065.1:c.-243+3952A=	NP_001171536.1:n.-243+3952A=
XM_005247836.2:c.-243+4299A=	XP_005247893.1:n.-243+4299A=
XM_006713789.2:c.-243+3952A=	XP_006713852.1:n.-243+3952A=
XM_011513237.1:c.-2263+3952A=	XP_011511539.1:n.-2263+3952A=
XM_011513238.1:c.-2263+4669A=	XP_011511540.1:n.-2263+4669A=
XM_006713789.3:c.-243+3952A=	XP_006713852.1:n.-243+3952A=
NM_000388.4:c.-243+4669A= MANE Select	NP_000379.3:n.-243+4669A=
NM_001178065.2:c.-243+3952A=	NP_001171536.2:n.-243+3952A=