Canonical Allele Identifier: CA368990568
Gene: CFTR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117610571A>C , CM000669.2:g.117610571A>C GRCh38
NC_000007.13:g.117250625A>C , CM000669.1:g.117250625A>C GRCh37
NC_000007.12:g.117037861A>C NCBI36
NG_016465.4:g.149788A>C , LRG_663:g.149788A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000647720.2:c.3041A>C ENSP00000497673.2:p.Tyr1014Ser
ENST00000647978.2:c.*2755A>C ENSP00000497658.1:n.*2755A>C
ENST00000649781.2:c.2858A>C ENSP00000497203.1:p.Tyr953Ser
ENST00000685018.2:c.3041A>C ENSP00000510194.2:p.Tyr1014Ser
ENST00000687278.2:c.3041A>C ENSP00000509593.2:p.Tyr1014Ser
ENST00000699585.1:c.3041A>C ENSP00000514456.1:p.Tyr1014Ser
ENST00000699598.1:c.3041A>C ENSP00000514467.1:p.Tyr1014Ser
ENST00000699599.1:c.3041A>C ENSP00000514468.1:p.Tyr1014Ser
ENST00000699600.1:c.3041A>C ENSP00000514469.1:p.Tyr1014Ser
ENST00000699601.1:c.*1341A>C ENSP00000514470.1:n.*1341A>C
ENST00000699602.1:c.3041A>C ENSP00000514471.1:p.Tyr1014Ser
ENST00000699604.1:c.*2865A>C ENSP00000514472.1:n.*2865A>C
ENST00000699605.1:c.2615A>C ENSP00000514473.1:p.Tyr872Ser
ENST00000687278.1:c.632A>C ENSP00000509593.1:p.Tyr211Ser
ENST00000003084.11:c.3041A>C MANE Select ENSP00000003084.6:p.Tyr1014Ser
ENST00000647720.1:c.691A>C
ENST00000648260.1:c.1823A>C ENSP00000497957.1:p.Tyr608Ser
ENST00000649406.1:c.2858A>C ENSP00000497965.1:p.Tyr953Ser
ENST00000649781.1:c.2858A>C ENSP00000497203.1:p.Tyr953Ser
ENST00000003084.10:c.3041A>C ENSP00000003084.6:p.Tyr1014Ser
ENST00000426809.5:c.2951A>C ENSP00000389119.1:p.Tyr984Ser
NM_000492.3:c.3041A>C , LRG_663t1:c.3041A>C NP_000483.3:p.Tyr1014Ser
XM_011515751.1:c.3131A>C XP_011514053.1:p.Tyr1044Ser
XM_011515752.1:c.3131A>C XP_011514054.1:p.Tyr1044Ser
XM_011515753.1:c.2798A>C XP_011514055.1:p.Tyr933Ser
XM_011515754.1:c.2798A>C XP_011514056.1:p.Tyr933Ser
NM_000492.4:c.3041A>C MANE Select NP_000483.3:p.Tyr1014Ser