Canonical Allele Identifier: CA354160742

Gene: CASR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122284730C>T , CM000665.2:g.122284730C>T	GRCh38
NC_000003.11:g.122003577C>T , CM000665.1:g.122003577C>T	GRCh37
NC_000003.10:g.123486267C>T	NCBI36
NG_009058.1:g.106048C>T
NG_009058.2:g.106063C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000388.4:c.2776C>T MANE Select	NP_000379.3:p.Gln926Ter
ENST00000639785.2:c.2776C>T MANE Select	ENSP00000491584.2:p.Gln926Ter
NM_000388.3:c.2776C>T	NP_000379.2:p.Gln926Ter
NM_001178065.1:c.2806C>T	NP_001171536.1:p.Gln936Ter
NM_001178065.2:c.2806C>T	NP_001171536.2:p.Gln936Ter
ENST00000490131.5:c.2776C>T	ENSP00000418685.1:p.Gln926Ter
ENST00000490131.7:c.2545C>T	ENSP00000418685.2:p.Gln849Ter
ENST00000498619.2:c.2806C>T	ENSP00000420194.1:p.Gln936Ter
ENST00000498619.4:c.2806C>T	ENSP00000420194.1:p.Gln936Ter
ENST00000638421.1:c.2776C>T	ENSP00000492190.1:p.Gln926Ter
XM_005247836.2:c.2776C>T	XP_005247893.1:p.Gln926Ter
XM_005247837.2:c.2293C>T	XP_005247894.1:p.Gln765Ter
XM_006713789.2:c.2776C>T	XP_006713852.1:p.Gln926Ter
XM_006713789.3:c.2776C>T	XP_006713852.1:p.Gln926Ter
XM_011513237.1:c.2776C>T	XP_011511539.1:p.Gln926Ter
XM_011513238.1:c.2776C>T	XP_011511540.1:p.Gln926Ter
XM_011513239.1:c.2188C>T	XP_011511541.1:p.Gln730Ter
XM_017007324.1:c.2776C>T	XP_016862813.1:p.Gln926Ter
XM_017007325.1:c.2776C>T	XP_016862814.1:p.Gln926Ter