Canonical Allele Identifier: CA2840613145

Gene: CASR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122283666C>A , CM000665.2:g.122283666C>A	GRCh38
NC_000003.11:g.122002513C>A , CM000665.1:g.122002513C>A	GRCh37
NC_000003.10:g.123485203C>A	NCBI36
NG_009058.1:g.104984C>A
NG_009058.2:g.104999C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490131.7:c.1502-21C>A	ENSP00000418685.2:n.1502-21C>A
ENST00000498619.4:c.1763-21C>A	ENSP00000420194.1:n.1763-21C>A
ENST00000638421.1:c.1733-21C>A	ENSP00000492190.1:n.1733-21C>A
ENST00000639785.2:c.1733-21C>A MANE Select	ENSP00000491584.2:n.1733-21C>A
ENST00000490131.5:c.1733-21C>A	ENSP00000418685.1:n.1733-21C>A
ENST00000498619.2:c.1763-21C>A	ENSP00000420194.1:n.1763-21C>A
NM_000388.3:c.1733-21C>A	NP_000379.2:n.1733-21C>A
NM_001178065.1:c.1763-21C>A	NP_001171536.1:n.1763-21C>A
XM_005247836.2:c.1733-21C>A	XP_005247893.1:n.1733-21C>A
XM_005247837.2:c.1250-21C>A	XP_005247894.1:n.1250-21C>A
XM_006713789.2:c.1733-21C>A	XP_006713852.1:n.1733-21C>A
XM_011513237.1:c.1733-21C>A	XP_011511539.1:n.1733-21C>A
XM_011513238.1:c.1733-21C>A	XP_011511540.1:n.1733-21C>A
XM_011513239.1:c.1145-21C>A	XP_011511541.1:n.1145-21C>A
XM_006713789.3:c.1733-21C>A	XP_006713852.1:n.1733-21C>A
XM_017007324.1:c.1733-21C>A	XP_016862813.1:n.1733-21C>A
XM_017007325.1:c.1733-21C>A	XP_016862814.1:n.1733-21C>A
NM_000388.4:c.1733-21C>A MANE Select	NP_000379.3:n.1733-21C>A
NM_001178065.2:c.1763-21C>A	NP_001171536.2:n.1763-21C>A