Canonical Allele Identifier: CA6746027

Gene: SYCP3 CHPT1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101737918T>A , CM000674.2:g.101737918T>A	GRCh38
NC_000012.11:g.102131696T>A , CM000674.1:g.102131696T>A	GRCh37
NC_000012.10:g.100655827T>A	NCBI36
NG_021181.1:g.6552A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392924.2:c.18A>T (SYCP3) MANE Select	ENSP00000376655.1:p.Lys6Asn
ENST00000266743.6:c.18A>T (SYCP3)	ENSP00000266743.2:p.Lys6Asn
ENST00000392924.1:c.18A>T (SYCP3)	ENSP00000376655.1:p.Lys6Asn
ENST00000392927.7:c.18A>T (SYCP3)	ENSP00000376658.3:p.Lys6Asn
ENST00000478139.1:n.146A>T (SYCP3)
ENST00000546873.1:c.199-5797T>A (CHPT1)
NM_001177948.1:c.18A>T (SYCP3)	NP_001171419.1:p.Lys6Asn
NM_001177949.1:c.18A>T (SYCP3)	NP_001171420.1:p.Lys6Asn
NM_153694.4:c.18A>T (SYCP3)	NP_710161.1:p.Lys6Asn
XM_005268922.3:c.189A>T (SYCP3)	XP_005268979.2:p.Lys63Asn
XM_005268924.1:c.18A>T (SYCP3)	XP_005268981.1:p.Lys6Asn
XM_005268925.1:c.18A>T (SYCP3)	XP_005268982.1:p.Lys6Asn
XM_005268926.3:c.18A>T (SYCP3)	XP_005268983.1:p.Lys6Asn
XM_005268927.2:c.18A>T (SYCP3)	XP_005268984.1:p.Lys6Asn
XM_011538421.1:c.18A>T (SYCP3)	XP_011536723.1:p.Lys6Asn
XR_945267.1:n.45-4479T>A
XM_005268922.5:c.258A>T (SYCP3)	XP_005268979.3:p.Lys86Asn
XM_005268926.4:c.18A>T (SYCP3)	XP_005268983.1:p.Lys6Asn
XM_011538421.3:c.180A>T (SYCP3)	XP_011536723.2:p.Lys60Asn
XM_017019368.2:c.258A>T (SYCP3)	XP_016874857.1:p.Lys86Asn
XM_024448994.1:c.18A>T (SYCP3)	XP_024304762.1:p.Lys6Asn
XM_024448995.1:c.18A>T (SYCP3)	XP_024304763.1:p.Lys6Asn
XM_024448996.1:c.18A>T (SYCP3)	XP_024304764.1:p.Lys6Asn
XR_001748816.1:n.1483-4479T>A (CHPT1)
XR_001748817.1:n.1483-4479T>A (CHPT1)
NM_001177949.2:c.18A>T (SYCP3) MANE Select	NP_001171420.1:p.Lys6Asn
NM_001177948.2:c.18A>T (SYCP3)	NP_001171419.1:p.Lys6Asn
NM_153694.5:c.18A>T (SYCP3)	NP_710161.1:p.Lys6Asn