Canonical Allele Identifier: CA2628140747

Gene: CKMT1B STRC

Linked Data

• gnomAD v4: 15-43599393-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43599393C>T , CM000677.2:g.43599393C>T	GRCh38
NC_000015.9:g.43891591C>T , CM000677.1:g.43891591C>T	GRCh37
NC_000015.8:g.41678883C>T	NCBI36
NG_011636.1:g.24408G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000441322.6:c.*120C>T (CKMT1B) MANE Select	ENSP00000413255.2:n.*120C>T
ENST00000300283.10:c.*120C>T (CKMT1B)	ENSP00000300283.6:n.*120C>T
ENST00000411560.1:n.2C>T (CKMT1B)
ENST00000437534.3:c.*1294C>T (CKMT1B)	ENSP00000416717.1:n.*1294C>T
ENST00000441322.5:c.*120C>T (CKMT1B)	ENSP00000413255.1:n.*120C>T
NM_020990.3:c.*120C>T (CKMT1B)	NP_066270.1:n.*120C>T
XM_005254150.3:c.*120C>T (CKMT1B)	XP_005254207.1:n.*120C>T
XM_011521194.1:c.*120C>T (CKMT1B)	XP_011519496.1:n.*120C>T
XM_011521195.1:c.*120C>T (CKMT1B)	XP_011519497.1:n.*120C>T
XM_011521196.1:c.*120C>T (CKMT1B)	XP_011519498.1:n.*120C>T
XM_011521197.1:c.*120C>T (CKMT1B)	XP_011519499.1:n.*120C>T
XM_011521198.1:c.*120C>T (CKMT1B)	XP_011519500.1:n.*120C>T
XM_011521277.1:c.*279G>A (STRC)	XP_011519579.1:n.*279G>A
XM_011521278.1:c.*279G>A (STRC)	XP_011519580.1:n.*279G>A
XM_011521279.1:c.*279G>A (STRC)	XP_011519581.1:n.*279G>A
NM_020990.4:c.*120C>T (CKMT1B)	NP_066270.1:n.*120C>T
NR_135748.1:n.2829C>T (CKMT1B)
NR_135749.1:n.2809C>T (CKMT1B)
NR_135750.1:n.2780C>T (CKMT1B)
NR_135751.1:n.2669C>T (CKMT1B)
NR_135752.1:n.2436C>T (CKMT1B)
XM_005254150.4:c.*120C>T (CKMT1B)	XP_005254207.1:n.*120C>T
XM_011521195.2:c.*120C>T (CKMT1B)	XP_011519497.1:n.*120C>T
XM_011521197.2:c.*120C>T (CKMT1B)	XP_011519499.1:n.*120C>T
XM_011521199.2:c.*120C>T (CKMT1B)	XP_011519501.2:n.*120C>T
XM_017021902.1:c.*120C>T (CKMT1B)	XP_016877391.1:n.*120C>T
NM_001375484.1:c.*120C>T (CKMT1B) MANE Select	NP_001362413.1:n.*120C>T
NM_020990.5:c.*120C>T (CKMT1B)	NP_066270.1:n.*120C>T
NR_135750.2:n.2780C>T (CKMT1B)