Canonical Allele Identifier: CA62593103
Gene: ANKAR HGNC NCBI

Linked Data

dbSNP Id: rs12053254

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189742427T>C , CM000664.2:g.189742427T>C GRCh38
NC_000002.11:g.190607153T>C , CM000664.1:g.190607153T>C GRCh37
NC_000002.10:g.190315398T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000684021.1:c.3811-848T>C MANE Select ENSP00000507233.1:n.3811-848T>C
ENST00000313581.4:c.3811-848T>C ENSP00000313513.4:n.3811-848T>C
ENST00000433782.6:c.*337+976T>C ENSP00000399928.2:n.*337+976T>C
ENST00000441800.5:c.*338-848T>C ENSP00000407459.1:n.*338-848T>C
ENST00000474303.5:n.340+976T>C
ENST00000476208.1:n.234+976T>C
ENST00000520309.5:c.3811-848T>C ENSP00000427882.1:n.3811-848T>C
NM_144708.3:c.3811-848T>C NP_653309.3:n.3811-848T>C
XM_011510673.1:c.3844-848T>C XP_011508975.1:n.3844-848T>C
XM_011510674.1:c.3811-848T>C XP_011508976.1:n.3811-848T>C
XM_011510675.1:c.3739-848T>C XP_011508977.1:n.3739-848T>C
XM_011510676.1:c.3844-848T>C XP_011508978.1:n.3844-848T>C
XM_011510677.1:c.3844-848T>C XP_011508979.1:n.3844-848T>C
XM_011510678.1:c.3844-848T>C XP_011508980.1:n.3844-848T>C
XM_011510679.1:c.3415-848T>C XP_011508981.1:n.3415-848T>C
XM_011510680.1:c.3843+976T>C XP_011508982.1:n.3843+976T>C
XM_011510681.1:c.3843+976T>C XP_011508983.1:n.3843+976T>C
XM_011510682.1:c.3843+976T>C XP_011508984.1:n.3843+976T>C
XM_011510683.1:c.3843+976T>C XP_011508985.1:n.3843+976T>C
XM_011510684.1:c.3843+976T>C XP_011508986.1:n.3843+976T>C
XM_011510685.1:c.3388-848T>C XP_011508987.1:n.3388-848T>C
XM_011510686.1:c.3337-848T>C XP_011508988.1:n.3337-848T>C
XM_011510687.1:c.3136-848T>C XP_011508989.1:n.3136-848T>C
XM_011510691.1:c.2599-848T>C XP_011508993.1:n.2599-848T>C
XM_011510692.1:c.2557-848T>C XP_011508994.1:n.2557-848T>C
XM_011510693.1:c.2368-848T>C XP_011508995.1:n.2368-848T>C
XM_011510694.1:c.2341-848T>C XP_011508996.1:n.2341-848T>C
XR_922866.1:n.4187+976T>C
XM_011510673.2:c.3844-848T>C XP_011508975.1:n.3844-848T>C
XM_011510675.2:c.3739-848T>C XP_011508977.1:n.3739-848T>C
XM_011510676.2:c.3844-848T>C XP_011508978.1:n.3844-848T>C
XM_011510677.2:c.3844-848T>C XP_011508979.1:n.3844-848T>C
XM_011510679.2:c.3415-848T>C XP_011508981.1:n.3415-848T>C
XM_011510682.2:c.3843+976T>C XP_011508984.1:n.3843+976T>C
XM_011510685.2:c.3388-848T>C XP_011508987.1:n.3388-848T>C
XM_011510686.2:c.3337-848T>C XP_011508988.1:n.3337-848T>C
XM_011510687.2:c.3136-848T>C XP_011508989.1:n.3136-848T>C
XM_011510691.2:c.2599-848T>C XP_011508993.1:n.2599-848T>C
XM_011510692.2:c.2557-848T>C XP_011508994.1:n.2557-848T>C
XM_011510693.2:c.2368-848T>C XP_011508995.1:n.2368-848T>C
XM_011510694.2:c.2341-848T>C XP_011508996.1:n.2341-848T>C
XM_017003413.1:c.3843+976T>C XP_016858902.1:n.3843+976T>C
XM_017003415.1:c.2467-848T>C XP_016858904.1:n.2467-848T>C
XM_017003416.1:c.2341-848T>C XP_016858905.1:n.2341-848T>C
XM_017003418.1:c.2236-848T>C XP_016858907.1:n.2236-848T>C
XM_017003419.1:c.2203-848T>C XP_016858908.1:n.2203-848T>C
XM_017003420.1:c.1723-848T>C XP_016858909.1:n.1723-848T>C
XM_024452718.1:c.3175-848T>C XP_024308486.1:n.3175-848T>C
XR_001738641.1:n.4154+976T>C
XR_001738643.1:n.3992+976T>C
XR_001738644.1:n.3887+976T>C
NM_001378068.1:c.3811-848T>C MANE Select NP_001364997.1:n.3811-848T>C