Canonical Allele Identifier: CA101734377

Gene: CCSER1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.90907222C>A , CM000666.2:g.90907222C>A	GRCh38
NC_000004.11:g.91828373C>A , CM000666.1:g.91828373C>A	GRCh37
NC_000004.10:g.92047396C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001145065.2:c.2095-16148C>A MANE Select	NP_001138537.1:n.2095-16148C>A
ENST00000509176.6:c.2095-16148C>A MANE Select	ENSP00000425040.1:n.2095-16148C>A
NM_001145065.1:c.2095-16148C>A	NP_001138537.1:n.2095-16148C>A
NM_001377987.1:c.2095-16148C>A	NP_001364916.1:n.2095-16148C>A
ENST00000503421.5:c.154-4033C>A	ENSP00000421678.1:n.154-4033C>A
ENST00000505073.5:c.*194-16148C>A	ENSP00000420964.1:n.*194-16148C>A
ENST00000509109.5:c.154-4033C>A	ENSP00000421693.1:n.154-4033C>A
ENST00000509176.5:c.2095-16148C>A	ENSP00000425040.1:n.2095-16148C>A
ENST00000513522.5:c.371-16148C>A
ENST00000515693.1:n.34-4033C>A
XM_011531936.1:c.2191-16148C>A	XP_011530238.1:n.2191-16148C>A
XM_011531937.1:c.2191-16148C>A	XP_011530239.1:n.2191-16148C>A
XM_011531937.2:c.2191-16148C>A	XP_011530239.1:n.2191-16148C>A
XM_011531938.1:c.2191-16148C>A	XP_011530240.1:n.2191-16148C>A
XM_011531938.2:c.2191-16148C>A	XP_011530240.1:n.2191-16148C>A
XM_011531939.1:c.2191-16148C>A	XP_011530241.1:n.2191-16148C>A
XM_011531939.2:c.2191-16148C>A	XP_011530241.1:n.2191-16148C>A
XM_011531940.1:c.2113-16148C>A	XP_011530242.1:n.2113-16148C>A
XM_011531941.1:c.2191-16148C>A	XP_011530243.1:n.2191-16148C>A
XM_011531941.2:c.2191-16148C>A	XP_011530243.1:n.2191-16148C>A
XM_011531942.1:c.2191-16148C>A	XP_011530244.1:n.2191-16148C>A
XM_011531942.2:c.2191-16148C>A	XP_011530244.1:n.2191-16148C>A
XM_011531943.1:c.2191-16148C>A	XP_011530245.1:n.2191-16148C>A
XM_011531943.2:c.2191-16148C>A	XP_011530245.1:n.2191-16148C>A
XM_011531944.1:c.2191-16148C>A	XP_011530246.1:n.2191-16148C>A
XM_011531945.1:c.2191-11008C>A	XP_011530247.1:n.2191-11008C>A
XM_011531946.1:c.2191-11008C>A	XP_011530248.1:n.2191-11008C>A
XM_011531946.2:c.2191-11008C>A	XP_011530248.1:n.2191-11008C>A
XM_011531947.1:c.2191-11008C>A	XP_011530249.1:n.2191-11008C>A
XM_011531947.2:c.2191-11008C>A	XP_011530249.1:n.2191-11008C>A
XM_011531948.1:c.2191-16148C>A	XP_011530250.1:n.2191-16148C>A
XM_011531949.1:c.2191-16148C>A	XP_011530251.1:n.2191-16148C>A
XM_011531949.2:c.2191-16148C>A	XP_011530251.1:n.2191-16148C>A
XM_011531950.1:c.2191-16148C>A	XP_011530252.1:n.2191-16148C>A
XM_011531950.2:c.2191-16148C>A	XP_011530252.1:n.2191-16148C>A
XM_011531951.1:c.2191-16148C>A	XP_011530253.1:n.2191-16148C>A
XM_011531951.2:c.2191-16148C>A	XP_011530253.1:n.2191-16148C>A
XM_017008194.1:c.2191-16148C>A	XP_016863683.1:n.2191-16148C>A
XM_017008195.1:c.2191-16148C>A	XP_016863684.1:n.2191-16148C>A
XM_017008197.1:c.2095-16148C>A	XP_016863686.1:n.2095-16148C>A
XM_017008199.1:c.2095-16148C>A	XP_016863688.1:n.2095-16148C>A
XR_001741218.1:n.2670-11008C>A
XR_938731.1:n.2670-11008C>A
XR_938732.1:n.2670-11008C>A
XR_938733.1:n.2670-4033C>A
XR_938733.2:n.2670-4033C>A
XR_938734.1:n.2670-4033C>A
XR_938734.2:n.2670-4033C>A
XR_938735.1:n.2764-4033C>A
XR_938735.2:n.2764-4033C>A