Canonical Allele Identifier: CA675733855

Gene: KIAA1549L

Linked Data

• dbSNP Id: rs1335432938
• gnomAD v3: 11-33566594-T-C
• gnomAD v4: 11-33566594-T-C
• MyVariant Identifiers: chr11:g.33588140T>C (hg19) ; chr11:g.33566594T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.33566594T>C , CM000673.2:g.33566594T>C	GRCh38
NC_000011.9:g.33588140T>C , CM000673.1:g.33588140T>C	GRCh37
NC_000011.8:g.33544716T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000526400.7:c.1889-1482T>C	ENSP00000433481.3:n.1889-1482T>C
ENST00000265654.6:c.3330-1482T>C
ENST00000321505.9:c.3188-1482T>C	ENSP00000315295.4:n.3188-1482T>C
ENST00000526400.6:c.1889-1482T>C	ENSP00000433481.2:n.1889-1482T>C
ENST00000658780.2:c.4079-1482T>C MANE Select	ENSP00000499430.1:n.4079-1482T>C
ENST00000265654.5:c.3206-1482T>C	ENSP00000265654.5:n.3206-1482T>C
ENST00000321505.8:c.3188-1482T>C	ENSP00000315295.4:n.3188-1482T>C
ENST00000526400.5:c.1381-1482T>C
NM_012194.2:c.3188-1482T>C	NP_036326.2:n.3188-1482T>C
XM_005252847.2:c.3323-1482T>C	XP_005252904.2:n.3323-1482T>C
XM_005252848.2:c.3206-1482T>C	XP_005252905.1:n.3206-1482T>C
XM_011519969.1:c.3206-1482T>C	XP_011518271.1:n.3206-1482T>C
XM_011519970.1:c.1889-1482T>C	XP_011518272.1:n.1889-1482T>C
XM_005252847.3:c.3323-1482T>C	XP_005252904.2:n.3323-1482T>C
XM_005252848.3:c.3206-1482T>C	XP_005252905.1:n.3206-1482T>C
XM_011519969.2:c.3206-1482T>C	XP_011518271.1:n.3206-1482T>C
XM_011519970.2:c.1889-1482T>C	XP_011518272.1:n.1889-1482T>C
XM_017017484.2:c.3206-1482T>C	XP_016872973.1:n.3206-1482T>C
XM_017017486.1:c.1889-1482T>C	XP_016872975.1:n.1889-1482T>C
NM_012194.3:c.4079-1482T>C MANE Select	NP_036326.3:n.4079-1482T>C