Canonical Allele Identifier: CA1151976942

Gene: CAMTA1

Linked Data

• dbSNP Id: rs2095984627

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7664358_7664363del , CM000663.2:g.7664358_7664363del	GRCh38
NC_000001.10:g.7724418_7724423del , CM000663.1:g.7724418_7724423del	GRCh37
NC_000001.9:g.7647005_7647010del	NCBI36
NG_053148.1:g.884035_884040del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476864.2:c.1811_1816del	ENSP00000452319.2:p.His604_Ser605del
ENST00000700414.1:c.*1662_*1667del	ENSP00000514978.1:n.*1662_*1667del
ENST00000700415.1:c.1721_1726del	ENSP00000514979.1:p.His574_Ser575del
ENST00000700417.1:c.1739_1744del	ENSP00000514981.1:p.His580_Ser581del
ENST00000700419.1:c.74_79del	ENSP00000514983.1:p.His25_Ser26del
ENST00000700444.1:c.*1580_*1585del	ENSP00000514992.1:n.*1580_*1585del
ENST00000303635.12:c.1811_1816del MANE Select	ENSP00000306522.6:p.His604_Ser605del
ENST00000303635.11:c.1811_1816del	ENSP00000306522.6:p.His604_Ser605del
NM_015215.3:c.1811_1816del	NP_056030.1:p.His604_Ser605del
XM_011541083.1:c.1811_1816del	XP_011539385.1:p.His604_Ser605del
XM_011541084.1:c.1811_1816del	XP_011539386.1:p.His604_Ser605del
XM_011541085.1:c.1799_1804del	XP_011539387.1:p.His600_Ser601del
XM_011541086.1:c.1811_1816del	XP_011539388.1:p.His604_Ser605del
XM_011541087.1:c.1739_1744del	XP_011539389.1:p.His580_Ser581del
XM_011541088.1:c.1721_1726del	XP_011539390.1:p.His574_Ser575del
XM_011541089.1:c.1811_1816del	XP_011539391.1:p.His604_Ser605del
XM_011541090.1:c.1811_1816del	XP_011539392.1:p.His604_Ser605del
XM_011541091.1:c.1811_1816del	XP_011539393.1:p.His604_Ser605del
XM_011541092.1:c.1811_1816del	XP_011539394.1:p.His604_Ser605del
NM_001349608.1:c.1721_1726del	NP_001336537.1:p.His574_Ser575del
NM_001349609.1:c.1811_1816del	NP_001336538.1:p.His604_Ser605del
NM_001349610.1:c.1811_1816del	NP_001336539.1:p.His604_Ser605del
NM_001349612.1:c.1721_1726del	NP_001336541.1:p.His574_Ser575del
XM_011541083.2:c.1811_1816del	XP_011539385.1:p.His604_Ser605del
XM_011541084.2:c.1811_1816del	XP_011539386.1:p.His604_Ser605del
XM_011541086.3:c.1811_1816del	XP_011539388.1:p.His604_Ser605del
XM_011541087.2:c.1739_1744del	XP_011539389.1:p.His580_Ser581del
XM_011541088.2:c.1721_1726del	XP_011539390.1:p.His574_Ser575del
XM_011541090.3:c.1811_1816del	XP_011539392.1:p.His604_Ser605del
XM_011541091.2:c.1811_1816del	XP_011539393.1:p.His604_Ser605del
XM_011541092.3:c.1811_1816del	XP_011539394.1:p.His604_Ser605del
XM_017000774.2:c.1811_1816del	XP_016856263.1:p.His604_Ser605del
XM_017000777.1:c.1811_1816del	XP_016856266.1:p.His604_Ser605del
XM_017000778.1:c.1811_1816del	XP_016856267.1:p.His604_Ser605del
NM_015215.4:c.1811_1816del MANE Select	NP_056030.1:p.His604_Ser605del
NM_001349608.2:c.1721_1726del	NP_001336537.1:p.His574_Ser575del
NM_001349609.2:c.1811_1816del	NP_001336538.1:p.His604_Ser605del
NM_001349610.2:c.1811_1816del	NP_001336539.1:p.His604_Ser605del
NM_001349612.2:c.1721_1726del	NP_001336541.1:p.His574_Ser575del